Ignite Creation Date:
2025-12-25 @ 1:25 AM
Ignite Modification Date:
2025-12-28 @ 10:31 PM
Study NCT ID:
NCT00939393
Status:
COMPLETED
Last Update Posted:
2024-07-12
First Post:
2009-07-14
Is NOT Gene Therapy:
True
Has Adverse Events:
True
Brief Title:
Balloon Sinus Dilation In Office or OR
Sponsor:
Organization:
Raw JSON
{'hasResults': True, 'derivedSection': {'miscInfoModule': {'versionHolder': '2025-12-24'}}, 'resultsSection': {'moreInfoModule': {'pointOfContact': {'email': 'lenglan1@its.jnj.com', 'phone': '650-687-5888', 'title': 'Clinical Director', 'organization': 'Acclarent, Inc.'}, 'certainAgreement': {'restrictionType': 'GT60', 'piSponsorEmployee': False, 'restrictiveAgreement': True}}, 'adverseEventsModule': {'timeFrame': '1 year', 'description': 'Adverse event assessment by physician according to defined follow-up visit schedule, and by patient self-reporting.', 'eventGroups': [{'id': 'EG000', 'title': 'Office', 'description': "Endoscopic sinus surgery performed in physician's office using balloon sinus dilation device.", 'otherNumAtRisk': 37, 'otherNumAffected': 1, 'seriousNumAtRisk': 37, 'seriousNumAffected': 0}, {'id': 'EG001', 'title': 'Operating Room', 'description': 'Endoscopic sinus surgery performed in the operating room (OR) with or without balloon sinus dilation devices.', 'otherNumAtRisk': 35, 'otherNumAffected': 1, 'seriousNumAtRisk': 35, 'seriousNumAffected': 0}], 'otherEvents': [{'term': 'Epistaxis', 'notes': 'Adverse event assessment by physician according to defined follow-up visit schedule, and by patient self-reporting.', 'stats': [{'groupId': 'EG000', 'numAtRisk': 37, 'numEvents': 0, 'numAffected': 0}, {'groupId': 'EG001', 'numAtRisk': 35, 'numEvents': 1, 'numAffected': 1}], 'organSystem': 'Respiratory, thoracic and mediastinal disorders', 'assessmentType': 'SYSTEMATIC_ASSESSMENT'}, {'term': 'Swallowed pledget', 'notes': 'Adverse event assessment by physician according to defined follow-up visit schedule, and by patient self-reporting.', 'stats': [{'groupId': 'EG000', 'numAtRisk': 37, 'numEvents': 1, 'numAffected': 1}, {'groupId': 'EG001', 'numAtRisk': 35, 'numEvents': 0, 'numAffected': 0}], 'organSystem': 'Gastrointestinal disorders', 'assessmentType': 'SYSTEMATIC_ASSESSMENT'}], 'frequencyThreshold': '0'}, 'outcomeMeasuresModule': {'outcomeMeasures': [{'type': 'SECONDARY', 'title': 'Mean Intra-patient Change in Lund-MacKay CT Score [24 Weeks]', 'denoms': [{'units': 'Participants', 'counts': [{'value': '29', 'groupId': 'OG000'}, {'value': '20', 'groupId': 'OG001'}]}], 'groups': [{'id': 'OG000', 'title': 'In Office', 'description': "Endoscopic sinus surgery performed in physician's office using balloon sinus dilation device."}, {'id': 'OG001', 'title': 'Operating Room', 'description': 'Endoscopic sinus surgery performed in the operating room (OR) with or without balloon sinus dilation devices.'}], 'classes': [{'categories': [{'measurements': [{'value': '-3.83', 'spread': '4.08', 'groupId': 'OG000'}, {'value': '-5.65', 'spread': '5.27', 'groupId': 'OG001'}]}]}], 'paramType': 'MEAN', 'timeFrame': '24 weeks', 'description': "The Lund-MacKay (LMK) CT (computed tomography) score is a scoring system to evaluate radiographic opacification of the paranasal sinuses. The LMK score will be evaluated at 24 weeks post-procedure compared to baseline. The LMK scoring system rates each of both the left and right frontal, maxillary, sphenoid, ostiomeatal complex, anterior ethmoid and posterior ethmoid sinuses on a scale of 0 to 2, where '0' is 'no opacification' and '2' is 'complete opacification'. The scores for a given subject are totaled and expressed as the LMK score, where zero is the minimum score, and 24 is the maximum score. A higher score represents greater sinus disease burden.", 'unitOfMeasure': 'Scores on a scale', 'dispersionType': 'Standard Deviation', 'reportingStatus': 'POSTED', 'populationDescription': 'Eight (8) In-Office subjects and 15 Operating Room subjects were missing data for this outcome measure.'}, {'type': 'SECONDARY', 'title': 'Proportion of Participants Rating Procedure as Tolerable (IO Only)', 'denoms': [{'units': 'Participants', 'counts': [{'value': '29', 'groupId': 'OG000'}]}], 'groups': [{'id': 'OG000', 'title': 'In Office', 'description': "Endoscopic sinus surgery performed in physician's office using balloon sinus dilation device."}], 'classes': [{'categories': [{'measurements': [{'value': '27', 'groupId': 'OG000'}]}]}], 'paramType': 'NUMBER', 'timeFrame': 'Day 0', 'description': "Participants evaluated the tolerability of their balloon dilation in office (IO = In Office) procedure on a scale from zero to 5, where '0' represented 'not tolerated' and '5' represented 'highly tolerable'. Scores of 3 through 5 were consdered tolerable ratings. The endpoint reports the proportion of participants rating the procedure as tolerable.", 'unitOfMeasure': 'participants', 'reportingStatus': 'POSTED', 'populationDescription': 'Eight (8) In-Office subjects were missing data for this outcome measure.'}, {'type': 'SECONDARY', 'title': 'Proportion of Participants Reporting No Pain or Pain of Low Intensity (IO Only)', 'denoms': [{'units': 'Participants', 'counts': [{'value': '36', 'groupId': 'OG000'}]}], 'groups': [{'id': 'OG000', 'title': 'In Office', 'description': "Endoscopic sinus surgery performed in physician's office using balloon sinus dilation device."}], 'classes': [{'categories': [{'measurements': [{'value': '24', 'groupId': 'OG000'}]}]}], 'paramType': 'NUMBER', 'timeFrame': 'Day 0', 'description': "Participants evaluated the per-procedural pain of their balloon dilation in office (IO = In Office) procedure on a scale from zero to 5, where '0' represented 'no pain' and '5' represented 'intense pain'. Scores of 0 through 2 were considered ratings of no pain or pain of low intensity. The endpoint reports the proportion of participants reporting no pain or pain of low intensity.", 'unitOfMeasure': 'participants', 'reportingStatus': 'POSTED', 'populationDescription': 'One (1) In-Office subject was missing data for this outcome measure.'}, {'type': 'SECONDARY', 'title': 'Mean Number of Debridements Per Participant (IO Only)', 'denoms': [{'units': 'Participants', 'counts': [{'value': '37', 'groupId': 'OG000'}]}], 'groups': [{'id': 'OG000', 'title': 'In Office', 'description': "Endoscopic sinus surgery performed in physician's office using balloon sinus dilation device."}], 'classes': [{'categories': [{'measurements': [{'value': '0.42', 'spread': '0.51', 'groupId': 'OG000'}]}]}], 'paramType': 'MEAN', 'timeFrame': '52 weeks', 'description': 'A debridement is a procedure to remove post-surgical crusts, mucus, and fibrin from obstructed nasal and sinus cavities after functional endoscopic sinus surgery. Each physician visit in which a debridement was performed was counted as one debridement.', 'unitOfMeasure': 'debridements', 'dispersionType': 'Standard Deviation', 'reportingStatus': 'POSTED'}, {'type': 'SECONDARY', 'title': 'Proportion of Participants With Revisions (IO Only)', 'denoms': [{'units': 'Participants', 'counts': [{'value': '37', 'groupId': 'OG000'}]}], 'groups': [{'id': 'OG000', 'title': 'In Office', 'description': "Endoscopic sinus surgery performed in physician's office using balloon sinus dilation device."}], 'classes': [{'categories': [{'measurements': [{'value': '1', 'groupId': 'OG000'}]}]}], 'paramType': 'NUMBER', 'timeFrame': '52 weeks', 'description': 'After sinus surgery, the patient may require a subsequent sinus procedure (a revision procedure) to address recurrence of disease. These revision procedures are assessed in this outcome measure.', 'unitOfMeasure': 'participants', 'reportingStatus': 'POSTED'}, {'type': 'SECONDARY', 'title': 'Proportion of Participants With Post-operative Sinus Infections', 'denoms': [{'units': 'Participants', 'counts': [{'value': '37', 'groupId': 'OG000'}, {'value': '35', 'groupId': 'OG001'}]}], 'groups': [{'id': 'OG000', 'title': 'In Office', 'description': "Endoscopic sinus surgery performed in physician's office using balloon sinus dilation device."}, {'id': 'OG001', 'title': 'Operating Room', 'description': 'Endoscopic sinus surgery performed in the operating room (OR) with or without balloon sinus dilation devices.'}], 'classes': [{'categories': [{'measurements': [{'value': '13', 'groupId': 'OG000'}, {'value': '12', 'groupId': 'OG001'}]}]}], 'paramType': 'NUMBER', 'timeFrame': '52 weeks', 'description': 'Investigators reported the sinus infections as secondary to chronic rhinosinusitis (CRS) or other pre-existing conditions such as allergies. The rates of these sinus infections are consistent with the disease burden of the subjects and consistent with post procedure symptomatology associated with endoscopic sinus surgery (ESS).', 'unitOfMeasure': 'participants', 'reportingStatus': 'POSTED'}, {'type': 'SECONDARY', 'title': 'Mean Intra-patient Change in SNOT-20 Score at 1 Week Post-procedure Compared to Baseline', 'denoms': [{'units': 'Participants', 'counts': [{'value': '32', 'groupId': 'OG000'}, {'value': '33', 'groupId': 'OG001'}]}], 'groups': [{'id': 'OG000', 'title': 'In Office', 'description': "Endoscopic sinus surgery performed in physician's office using balloon sinus dilation device."}, {'id': 'OG001', 'title': 'Operating Room', 'description': 'Endoscopic sinus surgery performed in the operating room (OR) with or without balloon sinus dilation devices.'}], 'classes': [{'categories': [{'measurements': [{'value': '-0.98', 'spread': '0.79', 'groupId': 'OG000'}, {'value': '-0.71', 'spread': '1.07', 'groupId': 'OG001'}]}]}], 'paramType': 'MEAN', 'timeFrame': '1 week', 'description': "The 20 question Sino-Nasal Outcome Test (SNOT-20) will be used to evaluate sinus symptoms and sinus-symptom related quality of life (QOL) at baseline, 1 week, 4 weeks, 24 weeks and 52 weeks post-procedure. The change in SNOT-20 score at each post-procedure time point will be evaluated compared to baseline SNOT-20 score. Each of the 20 questions in the SNOT-20 survey is scored on a scale of 0 to 5, where '0' represents 'no problem' and '5' represents 'problem as bad as it can be'. The 20 questions are expressed as a mean of the scores. Therefore, the minimum mean score is zero and the maximum mean score is 5.", 'unitOfMeasure': 'scores on a scale', 'dispersionType': 'Standard Deviation', 'reportingStatus': 'POSTED', 'populationDescription': 'Five (5) In-Office subjects and 2 Operating Room subjects were missing data for this outcome measure.'}, {'type': 'SECONDARY', 'title': 'Mean Intra-patient Change in SNOT-20 Score at 4 Weeks Post-procedure Compared to Baseline', 'denoms': [{'units': 'Participants', 'counts': [{'value': '31', 'groupId': 'OG000'}, {'value': '33', 'groupId': 'OG001'}]}], 'groups': [{'id': 'OG000', 'title': 'In Office', 'description': "Endoscopic sinus surgery performed in physician's office using balloon sinus dilation device."}, {'id': 'OG001', 'title': 'Operating Room', 'description': 'Endoscopic sinus surgery performed in the operating room (OR) with or without balloon sinus dilation devices.'}], 'classes': [{'categories': [{'measurements': [{'value': '-1.32', 'spread': '0.89', 'groupId': 'OG000'}, {'value': '-1.21', 'spread': '1.12', 'groupId': 'OG001'}]}]}], 'paramType': 'MEAN', 'timeFrame': '4 weeks', 'description': "The 20 question Sino-Nasal Outcome Test (SNOT-20) will be used to evaluate sinus symptoms and sinus-symptom related quality of life (QOL) at baseline, 1 week, 4 weeks, 24 weeks and 52 weeks post-procedure. The change in SNOT-20 score at each post-procedure time point will be evaluated compared to baseline SNOT-20 score. Each of the 20 questions in the SNOT-20 survey is scored on a scale of 0 to 5, where '0' represents 'no problem' and '5' represents 'problem as bad as it can be'. The 20 questions are expressed as a mean of the scores. Therefore, the minimum mean score is zero and the maximum mean score is 5.", 'unitOfMeasure': 'scores on a scale', 'dispersionType': 'Standard Deviation', 'reportingStatus': 'POSTED', 'populationDescription': 'Six (6) In-Office subjects and 2 Operating Room subjects were missing data for this outcome measure.'}, {'type': 'SECONDARY', 'title': 'Mean Intra-patient Change in SNOT-20 Score at 52 Weeks Post-procedure Compared to Baseline', 'denoms': [{'units': 'Participants', 'counts': [{'value': '21', 'groupId': 'OG000'}, {'value': '11', 'groupId': 'OG001'}]}], 'groups': [{'id': 'OG000', 'title': 'In Office', 'description': "Endoscopic sinus surgery performed in physician's office using balloon sinus dilation device."}, {'id': 'OG001', 'title': 'Operating Room', 'description': 'Endoscopic sinus surgery performed in the operating room (OR) with or without balloon sinus dilation devices.'}], 'classes': [{'categories': [{'measurements': [{'value': '-1.43', 'spread': '0.96', 'groupId': 'OG000'}, {'value': '-1.10', 'spread': '1.05', 'groupId': 'OG001'}]}]}], 'paramType': 'MEAN', 'timeFrame': '52 weeks', 'description': "The 20 question Sino-Nasal Outcome Test (SNOT-20) will be used to evaluate sinus symptoms and sinus-symptom related quality of life (QOL) at baseline, 1 week, 4 weeks, 24 weeks and 52 weeks post-procedure. The change in SNOT-20 score at each post-procedure time point will be evaluated compared to baseline SNOT-20 score. Each of the 20 questions in the SNOT-20 survey is scored on a scale of 0 to 5, where '0' represents 'no problem' and '5' represents 'problem as bad as it can be'. The 20 questions are expressed as a mean of the scores. Therefore, the minimum mean score is zero and the maximum mean score is 5.", 'unitOfMeasure': 'scores on a scale', 'dispersionType': 'Standard Deviation', 'reportingStatus': 'POSTED', 'populationDescription': 'Sixteen (16) In-Office subjects and 24 Operating Room subjects were missing data for this outcome measure.'}, {'type': 'PRIMARY', 'title': 'Mean Intra-patient Change in SNOT-20 Score at 24 Weeks Post-procedure Compared to Baseline', 'denoms': [{'units': 'Participants', 'counts': [{'value': '26', 'groupId': 'OG000'}, {'value': '25', 'groupId': 'OG001'}]}], 'groups': [{'id': 'OG000', 'title': 'In Office', 'description': "Endoscopic sinus surgery (ESS) performed in physician's office (IO, or In Office) using balloon sinus dilation device."}, {'id': 'OG001', 'title': 'Operating Room', 'description': 'Endoscopic sinus surgery (ESS) performed in the operating room (OR) with or without balloon sinus dilation devices.'}], 'classes': [{'categories': [{'measurements': [{'value': '-1.25', 'spread': '0.99', 'groupId': 'OG000'}, {'value': '-1.35', 'spread': '1.12', 'groupId': 'OG001'}]}]}], 'paramType': 'MEAN', 'timeFrame': '24 weeks', 'description': "The 20 question Sino-Nasal Outcome Test (SNOT-20) will be used to evaluate sinus symptoms and sinus-symptom related quality of life (QOL) at baseline, 1 week, 4 weeks, 24 weeks and 52 weeks post-procedure. The change in SNOT-20 score at each post-procedure time point will be evaluated compared to baseline SNOT-20 score. Each of the 20 questions in the SNOT-20 survey is scored on a scale of 0 to 5, where '0' represents 'no problem' and '5' represents 'problem as bad as it can be'. The 20 questions are expressed as a mean of the scores. Therefore, the minimum mean score is zero and the maximum mean score is 5.", 'unitOfMeasure': 'scores on a scale', 'dispersionType': 'Standard Deviation', 'reportingStatus': 'POSTED', 'populationDescription': 'Eleven (11) In-Office subjects and 10 Operating Room subjects were missing data for this outcome measure.'}]}, 'participantFlowModule': {'groups': [{'id': 'FG000', 'title': 'In Office', 'description': "Endoscopic sinus surgery performed in physician's office using balloon sinus dilation device."}, {'id': 'FG001', 'title': 'Operating Room', 'description': 'Endoscopic sinus surgery performed in the operating room (OR) with or without balloon sinus dilation devices.'}], 'periods': [{'title': 'Overall Study', 'milestones': [{'type': 'STARTED', 'achievements': [{'groupId': 'FG000', 'numSubjects': '37'}, {'groupId': 'FG001', 'numSubjects': '35'}]}, {'type': 'COMPLETED', 'achievements': [{'groupId': 'FG000', 'numSubjects': '33'}, {'groupId': 'FG001', 'numSubjects': '35'}]}, {'type': 'NOT COMPLETED', 'achievements': [{'groupId': 'FG000', 'numSubjects': '4'}, {'groupId': 'FG001', 'numSubjects': '0'}]}], 'dropWithdraws': [{'type': 'Withdrawal by Subject', 'reasons': [{'groupId': 'FG000', 'numSubjects': '1'}, {'groupId': 'FG001', 'numSubjects': '0'}]}, {'type': 'Lost to Follow-up', 'reasons': [{'groupId': 'FG000', 'numSubjects': '3'}, {'groupId': 'FG001', 'numSubjects': '0'}]}]}], 'recruitmentDetails': 'Eligible patients presenting to the study sites (medical clinics) for whom endoscopic sinus surgery was recommended were offered the opportunity to participate in the study by study investigators.'}, 'baselineCharacteristicsModule': {'denoms': [{'units': 'Participants', 'counts': [{'value': '37', 'groupId': 'BG000'}, {'value': '35', 'groupId': 'BG001'}, {'value': '72', 'groupId': 'BG002'}]}], 'groups': [{'id': 'BG000', 'title': 'Office', 'description': "Endoscopic sinus surgery performed in physician's office using balloon sinus dilation device."}, {'id': 'BG001', 'title': 'Operating Room', 'description': 'Endoscopic sinus surgery performed in the operating room (OR) with or without balloon sinus dilation devices.'}, {'id': 'BG002', 'title': 'Total', 'description': 'Total of all reporting groups'}], 'measures': [{'title': 'Age, Continuous', 'classes': [{'categories': [{'measurements': [{'value': '54.6', 'spread': '12.5', 'groupId': 'BG000'}, {'value': '47.5', 'spread': '15.1', 'groupId': 'BG001'}, {'value': '51.2', 'spread': '14.2', 'groupId': 'BG002'}]}]}], 'paramType': 'MEAN', 'unitOfMeasure': 'years', 'dispersionType': 'STANDARD_DEVIATION'}, {'title': 'Sex: Female, Male', 'classes': [{'categories': [{'title': 'Female', 'measurements': [{'value': '21', 'groupId': 'BG000'}, {'value': '23', 'groupId': 'BG001'}, {'value': '44', 'groupId': 'BG002'}]}, {'title': 'Male', 'measurements': [{'value': '16', 'groupId': 'BG000'}, {'value': '12', 'groupId': 'BG001'}, {'value': '28', 'groupId': 'BG002'}]}]}], 'paramType': 'COUNT_OF_PARTICIPANTS', 'unitOfMeasure': 'Participants'}, {'title': 'Region of Enrollment', 'classes': [{'title': 'United States', 'categories': [{'measurements': [{'value': '37', 'groupId': 'BG000'}, {'value': '35', 'groupId': 'BG001'}, {'value': '72', 'groupId': 'BG002'}]}]}], 'paramType': 'NUMBER', 'unitOfMeasure': 'participants'}]}}, 'protocolSection': {'designModule': {'phases': ['NA'], 'studyType': 'INTERVENTIONAL', 'designInfo': {'allocation': 'NON_RANDOMIZED', 'maskingInfo': {'masking': 'NONE'}, 'primaryPurpose': 'HEALTH_SERVICES_RESEARCH', 'interventionModel': 'PARALLEL'}, 'enrollmentInfo': {'type': 'ACTUAL', 'count': 72}}, 'statusModule': {'overallStatus': 'COMPLETED', 'startDateStruct': {'date': '2008-04-01', 'type': 'ACTUAL'}, 'expandedAccessInfo': {'hasExpandedAccess': False}, 'statusVerifiedDate': '2024-07', 'completionDateStruct': {'date': '2010-07-01', 'type': 'ACTUAL'}, 'lastUpdateSubmitDate': '2024-07-10', 'studyFirstSubmitDate': '2009-07-14', 'resultsFirstSubmitDate': '2014-05-06', 'studyFirstSubmitQcDate': '2009-07-14', 'lastUpdatePostDateStruct': {'date': '2024-07-12', 'type': 'ACTUAL'}, 'resultsFirstSubmitQcDate': '2014-09-29', 'studyFirstPostDateStruct': {'date': '2009-07-15', 'type': 'ESTIMATED'}, 'resultsFirstPostDateStruct': {'date': '2014-10-03', 'type': 'ESTIMATED'}, 'primaryCompletionDateStruct': {'date': '2009-06-01', 'type': 'ACTUAL'}}, 'outcomesModule': {'primaryOutcomes': [{'measure': 'Mean Intra-patient Change in SNOT-20 Score at 24 Weeks Post-procedure Compared to Baseline', 'timeFrame': '24 weeks', 'description': "The 20 question Sino-Nasal Outcome Test (SNOT-20) will be used to evaluate sinus symptoms and sinus-symptom related quality of life (QOL) at baseline, 1 week, 4 weeks, 24 weeks and 52 weeks post-procedure. The change in SNOT-20 score at each post-procedure time point will be evaluated compared to baseline SNOT-20 score. Each of the 20 questions in the SNOT-20 survey is scored on a scale of 0 to 5, where '0' represents 'no problem' and '5' represents 'problem as bad as it can be'. The 20 questions are expressed as a mean of the scores. Therefore, the minimum mean score is zero and the maximum mean score is 5."}], 'secondaryOutcomes': [{'measure': 'Mean Intra-patient Change in Lund-MacKay CT Score [24 Weeks]', 'timeFrame': '24 weeks', 'description': "The Lund-MacKay (LMK) CT (computed tomography) score is a scoring system to evaluate radiographic opacification of the paranasal sinuses. The LMK score will be evaluated at 24 weeks post-procedure compared to baseline. The LMK scoring system rates each of both the left and right frontal, maxillary, sphenoid, ostiomeatal complex, anterior ethmoid and posterior ethmoid sinuses on a scale of 0 to 2, where '0' is 'no opacification' and '2' is 'complete opacification'. The scores for a given subject are totaled and expressed as the LMK score, where zero is the minimum score, and 24 is the maximum score. A higher score represents greater sinus disease burden."}, {'measure': 'Proportion of Participants Rating Procedure as Tolerable (IO Only)', 'timeFrame': 'Day 0', 'description': "Participants evaluated the tolerability of their balloon dilation in office (IO = In Office) procedure on a scale from zero to 5, where '0' represented 'not tolerated' and '5' represented 'highly tolerable'. Scores of 3 through 5 were consdered tolerable ratings. The endpoint reports the proportion of participants rating the procedure as tolerable."}, {'measure': 'Proportion of Participants Reporting No Pain or Pain of Low Intensity (IO Only)', 'timeFrame': 'Day 0', 'description': "Participants evaluated the per-procedural pain of their balloon dilation in office (IO = In Office) procedure on a scale from zero to 5, where '0' represented 'no pain' and '5' represented 'intense pain'. Scores of 0 through 2 were considered ratings of no pain or pain of low intensity. The endpoint reports the proportion of participants reporting no pain or pain of low intensity."}, {'measure': 'Mean Number of Debridements Per Participant (IO Only)', 'timeFrame': '52 weeks', 'description': 'A debridement is a procedure to remove post-surgical crusts, mucus, and fibrin from obstructed nasal and sinus cavities after functional endoscopic sinus surgery. Each physician visit in which a debridement was performed was counted as one debridement.'}, {'measure': 'Proportion of Participants With Revisions (IO Only)', 'timeFrame': '52 weeks', 'description': 'After sinus surgery, the patient may require a subsequent sinus procedure (a revision procedure) to address recurrence of disease. These revision procedures are assessed in this outcome measure.'}, {'measure': 'Proportion of Participants With Post-operative Sinus Infections', 'timeFrame': '52 weeks', 'description': 'Investigators reported the sinus infections as secondary to chronic rhinosinusitis (CRS) or other pre-existing conditions such as allergies. The rates of these sinus infections are consistent with the disease burden of the subjects and consistent with post procedure symptomatology associated with endoscopic sinus surgery (ESS).'}, {'measure': 'Mean Intra-patient Change in SNOT-20 Score at 1 Week Post-procedure Compared to Baseline', 'timeFrame': '1 week', 'description': "The 20 question Sino-Nasal Outcome Test (SNOT-20) will be used to evaluate sinus symptoms and sinus-symptom related quality of life (QOL) at baseline, 1 week, 4 weeks, 24 weeks and 52 weeks post-procedure. The change in SNOT-20 score at each post-procedure time point will be evaluated compared to baseline SNOT-20 score. Each of the 20 questions in the SNOT-20 survey is scored on a scale of 0 to 5, where '0' represents 'no problem' and '5' represents 'problem as bad as it can be'. The 20 questions are expressed as a mean of the scores. Therefore, the minimum mean score is zero and the maximum mean score is 5."}, {'measure': 'Mean Intra-patient Change in SNOT-20 Score at 4 Weeks Post-procedure Compared to Baseline', 'timeFrame': '4 weeks', 'description': "The 20 question Sino-Nasal Outcome Test (SNOT-20) will be used to evaluate sinus symptoms and sinus-symptom related quality of life (QOL) at baseline, 1 week, 4 weeks, 24 weeks and 52 weeks post-procedure. The change in SNOT-20 score at each post-procedure time point will be evaluated compared to baseline SNOT-20 score. Each of the 20 questions in the SNOT-20 survey is scored on a scale of 0 to 5, where '0' represents 'no problem' and '5' represents 'problem as bad as it can be'. The 20 questions are expressed as a mean of the scores. Therefore, the minimum mean score is zero and the maximum mean score is 5."}, {'measure': 'Mean Intra-patient Change in SNOT-20 Score at 52 Weeks Post-procedure Compared to Baseline', 'timeFrame': '52 weeks', 'description': "The 20 question Sino-Nasal Outcome Test (SNOT-20) will be used to evaluate sinus symptoms and sinus-symptom related quality of life (QOL) at baseline, 1 week, 4 weeks, 24 weeks and 52 weeks post-procedure. The change in SNOT-20 score at each post-procedure time point will be evaluated compared to baseline SNOT-20 score. Each of the 20 questions in the SNOT-20 survey is scored on a scale of 0 to 5, where '0' represents 'no problem' and '5' represents 'problem as bad as it can be'. The 20 questions are expressed as a mean of the scores. Therefore, the minimum mean score is zero and the maximum mean score is 5."}]}, 'oversightModule': {'oversightHasDmc': False, 'isFdaRegulatedDrug': False, 'isFdaRegulatedDevice': True}, 'conditionsModule': {'conditions': ['Chronic Sinusitis']}, 'descriptionModule': {'briefSummary': "Endoscopic sinus surgery will be performed either in the physician's office or in the operating room (OR). Patients treated in the physician's office will have endoscopic sinus surgery performed with balloon sinuplasty devices. Patients treated in the OR will have endoscopic sinus surgery performed with or without balloon sinuplasty devices.", 'detailedDescription': "In this study, endoscopic sinus surgery will be performed either in the physician's office or in the operating room (OR). Patients treated in the physician's office will have endoscopic sinus surgery performed with the balloon sinuplasty devices. Patients treated in the OR will have endoscopic sinus surgery performed with or without balloon sinuplasty devices. Both primary treatment of sinusitis as well as revision of previously treated sinuses will be allowed. Resource absorption will be evaluated for both venues."}, 'eligibilityModule': {'sex': 'ALL', 'stdAges': ['ADULT', 'OLDER_ADULT'], 'minimumAge': '18 Years', 'healthyVolunteers': False, 'eligibilityCriteria': "Inclusion Criteria:\n\n1. Age 18 years and greater\n2. Both male and female patients eligible\n3. Diagnosis of chronic sinusitis that is not responsive to medical management (\\> 12 weeks of symptoms and failed at least 3 to 6 weeks of appropriate antibiotic therapy as evidenced by presence of disease on CT scan)\n4. Planned endoscopic sinus surgery (recommended by investigator, consented to by patient)\n\nExclusion Criteria:\n\n1. Cystic fibrosis\n2. Samter's Triad (Aspirin sensitivity, Asthma, Sinonasal polyposis)\n3. Sinonasal tumors or obstructive lesions\n4. History of facial trauma that distorts sinus anatomy and precludes access to the sinus ostium\n5. Ciliary dysfunction\n6. Pregnant females"}, 'identificationModule': {'nctId': 'NCT00939393', 'acronym': 'ORIOS', 'briefTitle': 'Balloon Sinus Dilation In Office or OR', 'organization': {'class': 'INDUSTRY', 'fullName': 'Integra LifeSciences Corporation'}, 'officialTitle': "ESS Performed in Operating Room Versus Clinician's Office", 'orgStudyIdInfo': {'id': 'CPR005002'}}, 'armsInterventionsModule': {'armGroups': [{'type': 'ACTIVE_COMPARATOR', 'label': 'FESS in OR with or without balloons', 'description': 'Functional Endoscopy Sinus Surgery', 'interventionNames': ['Device: FESS instruments with or without balloon treatment']}, {'type': 'ACTIVE_COMPARATOR', 'label': 'Balloon sinuplasty in physician office', 'description': 'Balloon Sinuplasty in physician office using Acclarent devices', 'interventionNames': ['Device: Balloon Sinuplasty']}], 'interventions': [{'name': 'FESS instruments with or without balloon treatment', 'type': 'DEVICE', 'description': 'Intervention with metal instruments with or without balloon treatment', 'armGroupLabels': ['FESS in OR with or without balloons']}, {'name': 'Balloon Sinuplasty', 'type': 'DEVICE', 'description': 'Balloon dilatation of sinuses', 'armGroupLabels': ['Balloon sinuplasty in physician office']}]}, 'contactsLocationsModule': {'locations': [{'zip': '44131', 'city': 'Independence', 'state': 'Ohio', 'country': 'United States', 'facility': 'Rockside Road Surgery Center', 'geoPoint': {'lat': 41.36866, 'lon': -81.6379}}], 'overallOfficials': [{'name': 'Howard Levine, MD', 'role': 'PRINCIPAL_INVESTIGATOR', 'affiliation': 'Rockside Road Surgery Center Independence, OH'}]}, 'ipdSharingStatementModule': {'ipdSharing': 'NO'}, 'sponsorCollaboratorsModule': {'leadSponsor': {'name': 'Integra LifeSciences Corporation', 'class': 'INDUSTRY'}, 'collaborators': [{'name': 'Acclarent', 'class': 'INDUSTRY'}], 'responsibleParty': {'type': 'SPONSOR'}}}}