Ignite Creation Date:
2025-12-24 @ 2:28 PM
Ignite Modification Date:
2026-02-25 @ 7:28 PM
Study NCT ID:
NCT01082159
Status:
COMPLETED
Last Update Posted:
2013-04-01
First Post:
2010-03-04
Is NOT Gene Therapy:
True
Has Adverse Events:
True
Brief Title:
MiDAS II (Mild® Decompression Alternative to Open Surgery): Vertos Mild Patient Evaluation Study
Sponsor:
Organization:
Raw JSON
{'hasResults': True, 'derivedSection': {'miscInfoModule': {'versionHolder': '2025-12-24'}, 'conditionBrowseModule': {'meshes': [{'id': 'D013130', 'term': 'Spinal Stenosis'}], 'ancestors': [{'id': 'D013122', 'term': 'Spinal Diseases'}, {'id': 'D001847', 'term': 'Bone Diseases'}, {'id': 'D009140', 'term': 'Musculoskeletal Diseases'}]}}, 'resultsSection': {'moreInfoModule': {'pointOfContact': {'email': 'cmyers@vertosmed.com', 'phone': '949-349-0008', 'title': 'VP Clinical Research', 'phoneExt': '216', 'organization': 'Vertos Medical'}, 'certainAgreement': {'restrictionType': 'LTE60', 'piSponsorEmployee': False, 'restrictiveAgreement': True}}, 'adverseEventsModule': {'timeFrame': 'Adverse events were collected from time of treatment through study period of six months.', 'eventGroups': [{'id': 'EG000', 'title': 'Lumbar Decompression', 'description': 'Single arm cohort having percutaneous decompression using the mild Device Kit', 'otherNumAtRisk': 55, 'otherNumAffected': 0, 'seriousNumAtRisk': 55, 'seriousNumAffected': 0}], 'frequencyThreshold': '0'}, 'outcomeMeasuresModule': {'outcomeMeasures': [{'type': 'PRIMARY', 'title': 'Changes in Back Pain as Measured by a 10-point Visual Analog Scale (VAS).', 'denoms': [{'units': 'Participants', 'counts': [{'value': '46', 'groupId': 'OG000'}]}], 'groups': [{'id': 'OG000', 'title': 'Lumbar Decompression', 'description': 'Single arm cohort having percutaneous decompression using the mild Device Kit'}], 'classes': [{'categories': [{'measurements': [{'value': '3.59', 'groupId': 'OG000', 'lowerLimit': '2.76', 'upperLimit': '4.42'}]}]}], 'analyses': [{'pValue': '<0.0001', 'groupIds': ['OG000'], 'paramType': 'change from baseline', 'ciNumSides': 'TWO_SIDED', 'ciPctValue': '95', 'paramValue': '3.59', 'ciLowerLimit': '2.76', 'ciUpperLimit': '4.42', 'dispersionType': 'STANDARD_DEVIATION', 'dispersionValue': '2.87', 'statisticalMethod': 't-test, 2 sided', 'nonInferiorityType': 'SUPERIORITY_OR_OTHER', 'testedNonInferiority': False}], 'paramType': 'MEAN', 'timeFrame': 'Baseline and Month 6', 'description': "The 10-point Visual Analog Scale (VAS)rates 'no pain' as zero and 'worst pain imaginable' as ten. VAS mean improvement greater than or equal to 2 points is considered clinically relevant.\n\nThe change from baseline to Month 6 is presented below where a positive value represents the baseline value minus the 6 month value.", 'unitOfMeasure': 'units on a scale', 'dispersionType': '95% Confidence Interval', 'reportingStatus': 'POSTED', 'populationDescription': 'All available participants who reported Month 6 outcomes are included in this analysis.'}, {'type': 'PRIMARY', 'title': 'Function as Measured Subjectively by the Oswestry Disability Index Questionnaire', 'denoms': [{'units': 'Participants', 'counts': [{'value': '46', 'groupId': 'OG000'}]}], 'groups': [{'id': 'OG000', 'title': 'Lumbar Decompression', 'description': 'Single arm cohort having percutaneous lumbar decompression using the mild Device Kit.'}], 'classes': [{'categories': [{'measurements': [{'value': '12.17', 'groupId': 'OG000', 'lowerLimit': '6.64', 'upperLimit': '17.71'}]}]}], 'analyses': [{'pValue': '<0.0001', 'groupIds': ['OG000'], 'paramType': 'Change from Baseline', 'ciNumSides': 'TWO_SIDED', 'ciPctValue': '95', 'paramValue': '12.17', 'ciLowerLimit': '6.64', 'ciUpperLimit': '17.71', 'dispersionType': 'STANDARD_DEVIATION', 'dispersionValue': '19.14', 'statisticalMethod': 't-test, 2 sided', 'nonInferiorityType': 'SUPERIORITY_OR_OTHER', 'testedNonInferiority': False}], 'paramType': 'MEAN', 'timeFrame': 'Baseline and Month 6', 'description': "Oswestry Disability Index (ODI) measures permanent functional disability using questions regarding activities of daily living (ADL), specifically disturbance of ADL related to chronic back pain. Higher scores indicate a 'more limited' life. The ten topics of the ODI are rated from zero (no pain/limitation) to five (high pain/very limited physically). The worst possible score is 50 (100% disability) with the best score being zero (0% disability).Change from baseline to 6 months is presented below, where a positive value represents the baseline value minus the 6 month value.", 'unitOfMeasure': 'units on a scale', 'dispersionType': '95% Confidence Interval', 'reportingStatus': 'POSTED', 'populationDescription': 'All available patients at 6 months are reported below.'}, {'type': 'PRIMARY', 'title': 'Quality of Life Changes as Determined by Short Form 12-question (SF-12) Survey Specifically Related to Physical Component Score (PCS).', 'denoms': [{'units': 'Participants', 'counts': [{'value': '42', 'groupId': 'OG000'}]}], 'groups': [{'id': 'OG000', 'title': 'Lumbar Decompression', 'description': 'Single arm cohort having percutaneous decompression using the mild Device Kit'}], 'classes': [{'categories': [{'measurements': [{'value': '8.32', 'groupId': 'OG000', 'lowerLimit': '5.72', 'upperLimit': '10.92'}]}]}], 'paramType': 'MEAN', 'timeFrame': 'Baseline and Month 6', 'description': 'The SF-12 is a validated norm-based scoring tool used to determine treatment outcomes. The PCS summary measure shows the impact of the treatment on the patients abilities to conduct their usual physical activities. Clinical relevance of PCS is established by baseline to post-treatment improvement of 2 to 3 points. Norm-based scoring is used so that each scale has the same mean (50 points) and the same standard deviation (10 points) as the general US population in 1998. Scores below 50 indicate a decline in health status, with lower scores representing worse health status. Minimally Important Difference (MID) is a measure of true clinical relevance of a difference, with suggested MID for the Physical Component Summary (PCS) being 2 to 3 points. Change from baseline to 6 months is presented, where a positive value represents the 6 month value minus the baseline value.', 'unitOfMeasure': 'units on a scale', 'dispersionType': '95% Confidence Interval', 'reportingStatus': 'POSTED', 'populationDescription': 'All participants at month 6 who completed all questionnaire fields necessary to analyze PCS data according to guidelines.'}]}, 'participantFlowModule': {'groups': [{'id': 'FG000', 'title': 'Lumbar Decompression', 'description': 'Single arm cohort having percutaneous decompression using the mild Device Kit'}], 'periods': [{'title': 'Overall Study', 'milestones': [{'type': 'STARTED', 'achievements': [{'groupId': 'FG000', 'numSubjects': '55'}]}, {'type': 'COMPLETED', 'achievements': [{'groupId': 'FG000', 'numSubjects': '46'}]}, {'type': 'NOT COMPLETED', 'achievements': [{'groupId': 'FG000', 'numSubjects': '9'}]}]}], 'recruitmentDetails': 'Patients were enrolled from July 2008 through January 2010.'}, 'baselineCharacteristicsModule': {'denoms': [{'units': 'Participants', 'counts': [{'value': '55', 'groupId': 'BG000'}]}], 'groups': [{'id': 'BG000', 'title': 'Lumbar Decompression', 'description': 'Single arm cohort having percutaneous decompression using the mild Device Kit'}], 'measures': [{'title': 'Age, Categorical', 'classes': [{'categories': [{'title': '<=18 years', 'measurements': [{'value': '0', 'groupId': 'BG000'}]}, {'title': 'Between 18 and 65 years', 'measurements': [{'value': '21', 'groupId': 'BG000'}]}, {'title': '>=65 years', 'measurements': [{'value': '34', 'groupId': 'BG000'}]}]}], 'paramType': 'COUNT_OF_PARTICIPANTS', 'unitOfMeasure': 'Participants'}, {'title': 'Age Continuous', 'classes': [{'categories': [{'measurements': [{'value': '68.3', 'spread': '12.1', 'groupId': 'BG000'}]}]}], 'paramType': 'MEAN', 'unitOfMeasure': 'years', 'dispersionType': 'STANDARD_DEVIATION'}, {'title': 'Sex: Female, Male', 'classes': [{'categories': [{'title': 'Female', 'measurements': [{'value': '32', 'groupId': 'BG000'}]}, {'title': 'Male', 'measurements': [{'value': '23', 'groupId': 'BG000'}]}]}], 'paramType': 'COUNT_OF_PARTICIPANTS', 'unitOfMeasure': 'Participants'}, {'title': 'Region of Enrollment', 'classes': [{'title': 'United States', 'categories': [{'measurements': [{'value': '55', 'groupId': 'BG000'}]}]}], 'paramType': 'NUMBER', 'unitOfMeasure': 'participants'}]}}, 'protocolSection': {'designModule': {'phases': ['PHASE4'], 'studyType': 'INTERVENTIONAL', 'designInfo': {'allocation': 'NA', 'maskingInfo': {'masking': 'NONE'}, 'primaryPurpose': 'TREATMENT', 'interventionModel': 'SINGLE_GROUP'}, 'enrollmentInfo': {'type': 'ACTUAL', 'count': 55}}, 'statusModule': {'overallStatus': 'COMPLETED', 'startDateStruct': {'date': '2010-02'}, 'expandedAccessInfo': {'hasExpandedAccess': False}, 'statusVerifiedDate': '2013-02', 'completionDateStruct': {'date': '2013-01', 'type': 'ACTUAL'}, 'lastUpdateSubmitDate': '2013-02-21', 'studyFirstSubmitDate': '2010-03-04', 'resultsFirstSubmitDate': '2013-02-15', 'studyFirstSubmitQcDate': '2010-03-05', 'lastUpdatePostDateStruct': {'date': '2013-04-01', 'type': 'ESTIMATED'}, 'resultsFirstSubmitQcDate': '2013-02-21', 'studyFirstPostDateStruct': {'date': '2010-03-08', 'type': 'ESTIMATED'}, 'resultsFirstPostDateStruct': {'date': '2013-04-01', 'type': 'ESTIMATED'}, 'primaryCompletionDateStruct': {'date': '2012-10', 'type': 'ACTUAL'}}, 'outcomesModule': {'primaryOutcomes': [{'measure': 'Changes in Back Pain as Measured by a 10-point Visual Analog Scale (VAS).', 'timeFrame': 'Baseline and Month 6', 'description': "The 10-point Visual Analog Scale (VAS)rates 'no pain' as zero and 'worst pain imaginable' as ten. VAS mean improvement greater than or equal to 2 points is considered clinically relevant.\n\nThe change from baseline to Month 6 is presented below where a positive value represents the baseline value minus the 6 month value."}, {'measure': 'Function as Measured Subjectively by the Oswestry Disability Index Questionnaire', 'timeFrame': 'Baseline and Month 6', 'description': "Oswestry Disability Index (ODI) measures permanent functional disability using questions regarding activities of daily living (ADL), specifically disturbance of ADL related to chronic back pain. Higher scores indicate a 'more limited' life. The ten topics of the ODI are rated from zero (no pain/limitation) to five (high pain/very limited physically). The worst possible score is 50 (100% disability) with the best score being zero (0% disability).Change from baseline to 6 months is presented below, where a positive value represents the baseline value minus the 6 month value."}, {'measure': 'Quality of Life Changes as Determined by Short Form 12-question (SF-12) Survey Specifically Related to Physical Component Score (PCS).', 'timeFrame': 'Baseline and Month 6', 'description': 'The SF-12 is a validated norm-based scoring tool used to determine treatment outcomes. The PCS summary measure shows the impact of the treatment on the patients abilities to conduct their usual physical activities. Clinical relevance of PCS is established by baseline to post-treatment improvement of 2 to 3 points. Norm-based scoring is used so that each scale has the same mean (50 points) and the same standard deviation (10 points) as the general US population in 1998. Scores below 50 indicate a decline in health status, with lower scores representing worse health status. Minimally Important Difference (MID) is a measure of true clinical relevance of a difference, with suggested MID for the Physical Component Summary (PCS) being 2 to 3 points. Change from baseline to 6 months is presented, where a positive value represents the 6 month value minus the baseline value.'}]}, 'oversightModule': {'oversightHasDmc': True}, 'conditionsModule': {'keywords': ['Spinal Stenosis', 'Lumbar Spinal Stenosis'], 'conditions': ['Lumbar Spinal Stenosis']}, 'descriptionModule': {'briefSummary': 'This is a multi-center, prospective, patient outcomes assessment of Minimally Invasive Lumbar Decompression with the Mild® devices in patients with symptomatic central canal spinal stenosis.'}, 'eligibilityModule': {'sex': 'ALL', 'stdAges': ['ADULT', 'OLDER_ADULT'], 'minimumAge': '18 Years', 'healthyVolunteers': False, 'eligibilityCriteria': "Inclusion Criteria:\n\n* Symptomatic lumbar spinal stenosis (LSS) primarily caused by dorsal element hypertrophy.\n* Prior failure of conservative therapy and Oswestry Disability Index (ODI) score \\> 20%.\n* Radiologic evidence of lumbar spinal stenosis (LSS), ligamentum flavum hypertrophy (typically \\> 2.5 mm), confirmed by pre-op MRI and/or CT.\n* Central canal cross sectional area clearly reduced per MRI/CT report.\n* If present, anterior listhesis preferred ≤ 5.0mm and deemed stable by Investigator.\n* Able to walk at least 10 feet unaided before being limited by pain.\n* Available to complete 26 weeks of follow-up.\n* A signed Informed Consent Form is obtained from the patient.\n* Adults at least 18 years of age.\n\nExclusion Criteria:\n\n* Prior surgery at intended treatment level.\n* Compound fracture with interspinal retropulsion contributing to spinal stenosis.\n* Disabling back or leg pain from causes other than LSS (e.g. acute compression fracture, metabolic neuropathy, or vascular claudication symptoms, etc.).\n* Disc protrusion or osteophyte formation severe enough to confound study outcome.\n* Facet hypertrophy severe enough to confound study outcome.\n* Bleeding disorders and/or current use of anti-coagulants.\n* Use of acetylsalicylic acid (ASA) and/or non-steroidal anti-inflammatory drug (NSAID) within 5 days of treatment.\n* Epidural steroid administration within prior three weeks (of procedure).\n* Inability of the patient to lie prone for any reason with anesthesia support (e.g.chronic obstructive pulmonary disease (COPD), obesity, etc.).\n* Metabolic wound healing pathologies deemed by Investigator to compromise study outcomes.\n* Dementia and/or inability to give informed consent.\n* Pregnant and/or breastfeeding.\n* On Workman's Compensation or considering litigation associated with back pain."}, 'identificationModule': {'nctId': 'NCT01082159', 'briefTitle': 'MiDAS II (Mild® Decompression Alternative to Open Surgery): Vertos Mild Patient Evaluation Study', 'organization': {'class': 'INDUSTRY', 'fullName': 'Vertos Medical, Inc.'}, 'officialTitle': 'MiDAS II (Mild® Decompression Alternative to Open Surgery): Vertos Mild Patient Evaluation Study', 'orgStudyIdInfo': {'id': 'MiDAS II'}}, 'armsInterventionsModule': {'armGroups': [{'type': 'OTHER', 'label': 'lumbar decompression', 'description': 'Percutaneous lumbar decompression with mild® Device Kit.', 'interventionNames': ['Procedure: lumbar decompression']}], 'interventions': [{'name': 'lumbar decompression', 'type': 'PROCEDURE', 'otherNames': ['The mild® Device Kit'], 'description': 'The mild® devices used in this study are specialized surgical instruments intended to be used to perform percutaneous lumbar decompressive procedures for the treatment of various spinal conditions.', 'armGroupLabels': ['lumbar decompression']}]}, 'contactsLocationsModule': {'locations': [{'zip': '32953', 'city': 'Merritt Island', 'state': 'Florida', 'country': 'United States', 'facility': 'Space Coast Pain Institute', 'geoPoint': {'lat': 28.359, 'lon': -80.69}}, {'zip': '21211', 'city': 'Baltimore', 'state': 'Maryland', 'country': 'United States', 'facility': 'The Spine Center', 'geoPoint': {'lat': 39.29038, 'lon': -76.61219}}, {'zip': '63028', 'city': 'Festus', 'state': 'Missouri', 'country': 'United States', 'facility': 'Occupational and Pain Management Professionals', 'geoPoint': {'lat': 38.22061, 'lon': -90.39595}}, {'zip': '89149', 'city': 'Las Vegas', 'state': 'Nevada', 'country': 'United States', 'facility': 'Lab2Marche, LLC', 'geoPoint': {'lat': 36.17497, 'lon': -115.13722}}, {'zip': '44195', 'city': 'Cleveland', 'state': 'Ohio', 'country': 'United States', 'facility': 'The Cleveland Clinic Foundation', 'geoPoint': {'lat': 41.4995, 'lon': -81.69541}}, {'zip': '44903', 'city': 'Mansfield', 'state': 'Ohio', 'country': 'United States', 'facility': 'MedCentral Health System', 'geoPoint': {'lat': 40.75839, 'lon': -82.51545}}, {'zip': '77090', 'city': 'Houston', 'state': 'Texas', 'country': 'United States', 'facility': 'Kenneth Alo, MD, PA-TX', 'geoPoint': {'lat': 29.76328, 'lon': -95.36327}}, {'zip': '25702', 'city': 'Huntington', 'state': 'West Virginia', 'country': 'United States', 'facility': 'The Center for Pain Relief Tri-State, PLLC', 'geoPoint': {'lat': 38.41925, 'lon': -82.44515}}], 'overallOfficials': [{'name': 'David L Caraway, MD, PhD', 'role': 'PRINCIPAL_INVESTIGATOR', 'affiliation': 'The Center for Pain Relief Tri-State, PLLC'}, {'name': 'Bohdan W Chopko, MD', 'role': 'PRINCIPAL_INVESTIGATOR', 'affiliation': 'MedCentral Health System'}]}, 'sponsorCollaboratorsModule': {'leadSponsor': {'name': 'Vertos Medical, Inc.', 'class': 'INDUSTRY'}, 'responsibleParty': {'type': 'SPONSOR'}}}}