Ignite Creation Date:
2025-12-24 @ 11:41 PM
Ignite Modification Date:
2025-12-25 @ 9:32 PM
Study NCT ID:
NCT04794751
Status:
COMPLETED
Last Update Posted:
2022-06-21
First Post:
2021-03-09
Is NOT Gene Therapy:
False
Has Adverse Events:
True
Brief Title:
Evaluation of Investigational Daily Disposable Multifocal Contact Lenses Produced With Different Manufacturing Processes
Sponsor:
Organization:
Raw JSON
{'hasResults': True, 'derivedSection': {'miscInfoModule': {'versionHolder': '2025-12-24'}}, 'resultsSection': {'moreInfoModule': {'pointOfContact': {'email': 'TKarkkai@its.jnj.com', 'phone': '1-800-843-2020', 'title': 'Thomas R. Karkkainen, OD, MS, FAAO', 'organization': 'Johnson & Johnson Vision Care, Inc.'}, 'certainAgreement': {'restrictionType': 'GT60', 'piSponsorEmployee': False, 'restrictiveAgreement': True}}, 'adverseEventsModule': {'timeFrame': 'Throughout the duration of the study; approximately 22-32 days per subject.', 'eventGroups': [{'id': 'EG000', 'title': 'Senofilcon A C3', 'description': 'Subjects that wore the Test lens in either of the three study periods.', 'otherNumAtRisk': 73, 'deathsNumAtRisk': 73, 'otherNumAffected': 0, 'seriousNumAtRisk': 73, 'deathsNumAffected': 0, 'seriousNumAffected': 0}, {'id': 'EG001', 'title': 'Delefilcon A', 'description': 'Subjects that wore the Control lens in either of the three study periods.', 'otherNumAtRisk': 70, 'deathsNumAtRisk': 70, 'otherNumAffected': 0, 'seriousNumAtRisk': 70, 'deathsNumAffected': 0, 'seriousNumAffected': 0}], 'frequencyThreshold': '5'}, 'outcomeMeasuresModule': {'outcomeMeasures': [{'type': 'PRIMARY', 'title': 'Visual Performance (logMAR)', 'denoms': [{'units': 'Participants', 'counts': [{'value': '64', 'groupId': 'OG000'}, {'value': '64', 'groupId': 'OG001'}]}], 'groups': [{'id': 'OG000', 'title': 'Senofilcon A C3', 'description': 'Subjects that wore the Test lens in either of the three study periods.'}, {'id': 'OG001', 'title': 'Delefilcon A', 'description': 'Subjects that wore the Control lens in either of the three study periods.'}], 'classes': [{'title': 'Distance (4m)', 'categories': [{'measurements': [{'value': '-0.08', 'spread': '0.068', 'groupId': 'OG000'}, {'value': '-0.06', 'spread': '0.081', 'groupId': 'OG001'}]}]}, {'title': 'Intermediate (64cm)', 'categories': [{'measurements': [{'value': '-0.01', 'spread': '0.096', 'groupId': 'OG000'}, {'value': '0.00', 'spread': '0.090', 'groupId': 'OG001'}]}]}, {'title': 'Near (40cm)', 'categories': [{'measurements': [{'value': '0.10', 'spread': '0.094', 'groupId': 'OG000'}, {'value': '0.09', 'spread': '0.089', 'groupId': 'OG001'}]}]}], 'analyses': [{'groupIds': ['OG000', 'OG001'], 'paramType': 'least-square mean difference', 'ciNumSides': 'TWO_SIDED', 'ciPctValue': '95', 'paramValue': '-0.018', 'ciLowerLimit': '-0.039', 'ciUpperLimit': '0.002', 'dispersionType': 'STANDARD_ERROR_OF_MEAN', 'dispersionValue': '0.0106', 'estimateComment': 'LS Mean difference was calculated as Test minus Control', 'groupDescription': 'Distance (4m)', 'statisticalMethod': 'Linear Mixed Model', 'nonInferiorityType': 'NON_INFERIORITY', 'statisticalComment': 'Linear mixed model using the Kenward and Roger method for the denominator degrees of freedom.', 'nonInferiorityComment': 'Non-Inferiority was declared if the upper limit of the 95% confidence interval of the LSM difference between the Test and Control was below 0.05 logMAR.'}, {'groupIds': ['OG000', 'OG001'], 'paramType': 'least-square mean difference', 'ciNumSides': 'TWO_SIDED', 'ciPctValue': '95', 'paramValue': '-0.007', 'ciLowerLimit': '-0.032', 'ciUpperLimit': '0.018', 'dispersionType': 'STANDARD_ERROR_OF_MEAN', 'dispersionValue': '0.0127', 'estimateComment': 'LS Mean difference was calculated as Test minus Control', 'groupDescription': 'Intermediate (64cm)', 'statisticalMethod': 'Linear Mixed Model', 'nonInferiorityType': 'NON_INFERIORITY', 'statisticalComment': 'Linear mixed model using the Kenward and Roger method for the denominator degrees of freedom.', 'nonInferiorityComment': 'Non-inferiority was declared if the upper limit of the 95% confidence interval of the LSM difference between the Test and Control was below 0.05 logMAR.'}, {'groupIds': ['OG000', 'OG001'], 'paramType': 'least-square mean difference', 'ciNumSides': 'TWO_SIDED', 'ciPctValue': '95', 'paramValue': '-0.010', 'ciLowerLimit': '-0.034', 'ciUpperLimit': '0.015', 'dispersionType': 'STANDARD_ERROR_OF_MEAN', 'dispersionValue': '0.0124', 'estimateComment': 'LS Mean difference was calculated as Test minus Control', 'groupDescription': 'Near (40cm)', 'statisticalMethod': 'Linear Mixed Model', 'nonInferiorityType': 'NON_INFERIORITY', 'statisticalComment': 'Linear mixed model using the Kenward and Roger method for the denominator degrees of freedom.', 'nonInferiorityComment': 'Non-inferiority was declared if the upper limit of the 95% confidence interval of the LSM difference between the Test and Control was below 0.05 logMAR.'}], 'paramType': 'MEAN', 'timeFrame': '1-Week Follow-up', 'description': 'Binocular visual performance on logMAR (Logarithm of Minimal Angle of Resolution) scale was evaluated at distance (4 m), intermediate (64 cm) and near (40 cm) under high luminance high contrast lighting conditions using ETDRS (Early Treatment Diabetic Retinopathy Study) charts. The room illuminance was required to be between 7.3 and 7.9 EV (394-597 lux). For Distance (4 m), the acceptable range for the chart luminance was 10.5-10.7 EV (181-208 cd/m2). For Intermediate (64cm) and Near (40cm), the cceptable range for the chart luminance 10.8-11.1 EV (223-274 cd/m2). Letter-by-letter results calculated the visual performance score for each chart read. logMAR scores closer to zero, or below zero, indicate a better visual acuity. A logMAR visual performance score of 0.0 is equivalent to Snellen visual acuity of 20/20. The average score was reported for each lens.', 'unitOfMeasure': 'logMAR', 'dispersionType': 'Standard Deviation', 'reportingStatus': 'POSTED', 'populationDescription': 'Subjects that completed all study visits, without a major protocol deviation impacting a primary or secondary endpoint.'}, {'type': 'SECONDARY', 'title': 'CLUE Vision', 'denoms': [{'units': 'Participants', 'counts': [{'value': '64', 'groupId': 'OG000'}, {'value': '64', 'groupId': 'OG001'}]}], 'groups': [{'id': 'OG000', 'title': 'Senofilcon A C3', 'description': 'Subjects that wore the Test lens in either of the three study periods.'}, {'id': 'OG001', 'title': 'Delefilcon A', 'description': 'Subjects that wore the Control lens in either of the three study periods.'}], 'classes': [{'categories': [{'measurements': [{'value': '55.34', 'spread': '20.468', 'groupId': 'OG000'}, {'value': '55.50', 'spread': '20.422', 'groupId': 'OG001'}]}]}], 'analyses': [{'groupIds': ['OG000', 'OG001'], 'paramType': 'least-square mean difference', 'ciNumSides': 'TWO_SIDED', 'ciPctValue': '95', 'paramValue': '0.1', 'ciLowerLimit': '-4.6', 'ciUpperLimit': '4.8', 'dispersionType': 'STANDARD_ERROR_OF_MEAN', 'dispersionValue': '2.34', 'estimateComment': 'LS Mean difference was calculated as Test minus Control', 'statisticalMethod': 'Linear Mixed Model', 'nonInferiorityType': 'NON_INFERIORITY', 'statisticalComment': 'Linear mixed model using the Kenward and Roger method for the denominator degrees of freedom.', 'nonInferiorityComment': 'Non-inferiority was declared if the lower limit of the 95% confidence interval for the least-square mean difference was greater than -5.'}], 'paramType': 'MEAN', 'timeFrame': '1-Week Follow-up', 'description': 'Subjective vision was assessed using the Contact Lens User Experience™ (CLUE) questionnaire. CLUE is a validated patient-reported outcomes (PRO) questionnaire to assess patient-experience attributes of soft contact lenses (comfort, vision, handling, and packaging) in a contact-lens wearing population in the US, ages 18-65. Derived CLUE scores using Item Response Theory (IRT) follow a normal distribution with a population average score of 60 (SD 20), where higher scores indicate a more favorable/positive response with a range of 0-120. The average CLUE vision score for each lens type was reported.', 'unitOfMeasure': 'units on a scale', 'dispersionType': 'Standard Deviation', 'reportingStatus': 'POSTED', 'populationDescription': 'Subjects that completed all study visits, without a major protocol deviation impacting a primary or secondary endpoint.'}]}, 'participantFlowModule': {'groups': [{'id': 'FG000', 'title': 'Delefilcon A/Senofilcon A C3/Senofilcon A C3', 'description': 'Subjects randomized to this sequence received the delefilcon A lens during the first period and then received the senofilcon A C3 lenses during the second and third periods.'}, {'id': 'FG001', 'title': 'Senofilcon A C3/Delefilcon A/Delefilcon A', 'description': 'Subjects randomized to this sequence received the senofilcon A C3 lens during the first period and then received the delefilcon A lenses during the second and third periods.'}], 'periods': [{'title': 'Period 1', 'milestones': [{'type': 'STARTED', 'achievements': [{'groupId': 'FG000', 'numSubjects': '38'}, {'groupId': 'FG001', 'numSubjects': '37'}]}, {'type': 'COMPLETED', 'achievements': [{'groupId': 'FG000', 'numSubjects': '36'}, {'groupId': 'FG001', 'numSubjects': '32'}]}, {'type': 'NOT COMPLETED', 'achievements': [{'groupId': 'FG000', 'numSubjects': '2'}, {'groupId': 'FG001', 'numSubjects': '5'}]}], 'dropWithdraws': [{'type': 'incorrect fitting guide was used to fit subject', 'reasons': [{'groupId': 'FG000', 'numSubjects': '2'}, {'groupId': 'FG001', 'numSubjects': '1'}]}, {'type': 'Subject no longer meets eligibility criteria', 'reasons': [{'groupId': 'FG000', 'numSubjects': '0'}, {'groupId': 'FG001', 'numSubjects': '1'}]}, {'type': 'Protocol Violation', 'reasons': [{'groupId': 'FG000', 'numSubjects': '0'}, {'groupId': 'FG001', 'numSubjects': '2'}]}, {'type': 'Withdrawal by Subject', 'reasons': [{'groupId': 'FG000', 'numSubjects': '0'}, {'groupId': 'FG001', 'numSubjects': '1'}]}]}, {'title': 'Period 2', 'milestones': [{'type': 'STARTED', 'achievements': [{'groupId': 'FG000', 'numSubjects': '36'}, {'groupId': 'FG001', 'numSubjects': '32'}]}, {'type': 'COMPLETED', 'achievements': [{'groupId': 'FG000', 'numSubjects': '35'}, {'groupId': 'FG001', 'numSubjects': '29'}]}, {'type': 'NOT COMPLETED', 'achievements': [{'groupId': 'FG000', 'numSubjects': '1'}, {'groupId': 'FG001', 'numSubjects': '3'}]}], 'dropWithdraws': [{'type': 'Withdrawal by Subject', 'reasons': [{'groupId': 'FG000', 'numSubjects': '0'}, {'groupId': 'FG001', 'numSubjects': '1'}]}, {'type': 'incorrect fitting guide was used to fit subject', 'reasons': [{'groupId': 'FG000', 'numSubjects': '0'}, {'groupId': 'FG001', 'numSubjects': '2'}]}, {'type': 'Protocol Violation', 'reasons': [{'groupId': 'FG000', 'numSubjects': '1'}, {'groupId': 'FG001', 'numSubjects': '0'}]}]}, {'title': 'Period 3', 'milestones': [{'type': 'STARTED', 'achievements': [{'groupId': 'FG000', 'numSubjects': '35'}, {'groupId': 'FG001', 'numSubjects': '29'}]}, {'type': 'COMPLETED', 'achievements': [{'groupId': 'FG000', 'numSubjects': '35'}, {'groupId': 'FG001', 'numSubjects': '29'}]}, {'type': 'NOT COMPLETED', 'achievements': [{'groupId': 'FG000', 'numSubjects': '0'}, {'groupId': 'FG001', 'numSubjects': '0'}]}]}], 'recruitmentDetails': 'In total, 78 subject were enrolled in this study. Of those enrolled, 75 subjects were dispensed at least one study lens while 3 subjects failed to meet all eligibility criteria. Of those who were assigned and administered a test article, 64 subjects completed the study while 11 subjects were discontinued.'}, 'baselineCharacteristicsModule': {'denoms': [{'units': 'Participants', 'counts': [{'value': '75', 'groupId': 'BG000'}]}], 'groups': [{'id': 'BG000', 'title': 'Dispensed Subjects', 'description': 'All subjects dispensed a study lens.'}], 'measures': [{'title': 'Age, Continuous', 'classes': [{'categories': [{'measurements': [{'value': '57.5', 'spread': '6.44', 'groupId': 'BG000'}]}]}], 'paramType': 'MEAN', 'unitOfMeasure': 'years', 'dispersionType': 'STANDARD_DEVIATION'}, {'title': 'Sex: Female, Male', 'classes': [{'categories': [{'title': 'Female', 'measurements': [{'value': '60', 'groupId': 'BG000'}]}, {'title': 'Male', 'measurements': [{'value': '15', 'groupId': 'BG000'}]}]}], 'paramType': 'COUNT_OF_PARTICIPANTS', 'unitOfMeasure': 'Participants'}, {'title': 'Race/Ethnicity, Customized', 'classes': [{'title': 'Black or African American', 'categories': [{'measurements': [{'value': '4', 'groupId': 'BG000'}]}]}, {'title': 'Native Hawaiian or Other Pacific Islander', 'categories': [{'measurements': [{'value': '2', 'groupId': 'BG000'}]}]}, {'title': 'White', 'categories': [{'measurements': [{'value': '69', 'groupId': 'BG000'}]}]}], 'paramType': 'NUMBER', 'unitOfMeasure': 'participants'}, {'title': 'Region of Enrollment', 'classes': [{'title': 'United States', 'categories': [{'measurements': [{'value': '75', 'groupId': 'BG000'}]}]}], 'paramType': 'COUNT_OF_PARTICIPANTS', 'unitOfMeasure': 'Participants'}], 'populationDescription': 'All subjects dispensed a study lens.'}}, 'documentSection': {'largeDocumentModule': {'largeDocs': [{'date': '2021-02-10', 'size': 9248651, 'label': 'Study Protocol and Statistical Analysis Plan', 'hasIcf': False, 'hasSap': True, 'filename': 'Prot_SAP_000.pdf', 'typeAbbrev': 'Prot_SAP', 'uploadDate': '2022-05-23T16:43', 'hasProtocol': True}]}}, 'protocolSection': {'designModule': {'phases': ['NA'], 'studyType': 'INTERVENTIONAL', 'designInfo': {'allocation': 'RANDOMIZED', 'maskingInfo': {'masking': 'SINGLE', 'whoMasked': ['PARTICIPANT']}, 'primaryPurpose': 'TREATMENT', 'interventionModel': 'CROSSOVER'}, 'enrollmentInfo': {'type': 'ACTUAL', 'count': 78}}, 'statusModule': {'overallStatus': 'COMPLETED', 'startDateStruct': {'date': '2021-03-13', 'type': 'ACTUAL'}, 'expandedAccessInfo': {'hasExpandedAccess': False}, 'statusVerifiedDate': '2022-05', 'completionDateStruct': {'date': '2021-06-10', 'type': 'ACTUAL'}, 'lastUpdateSubmitDate': '2022-05-23', 'studyFirstSubmitDate': '2021-03-09', 'resultsFirstSubmitDate': '2022-05-23', 'studyFirstSubmitQcDate': '2021-03-09', 'lastUpdatePostDateStruct': {'date': '2022-06-21', 'type': 'ACTUAL'}, 'resultsFirstSubmitQcDate': '2022-05-23', 'studyFirstPostDateStruct': {'date': '2021-03-12', 'type': 'ACTUAL'}, 'resultsFirstPostDateStruct': {'date': '2022-06-21', 'type': 'ACTUAL'}, 'primaryCompletionDateStruct': {'date': '2021-06-10', 'type': 'ACTUAL'}}, 'outcomesModule': {'primaryOutcomes': [{'measure': 'Visual Performance (logMAR)', 'timeFrame': '1-Week Follow-up', 'description': 'Binocular visual performance on logMAR (Logarithm of Minimal Angle of Resolution) scale was evaluated at distance (4 m), intermediate (64 cm) and near (40 cm) under high luminance high contrast lighting conditions using ETDRS (Early Treatment Diabetic Retinopathy Study) charts. The room illuminance was required to be between 7.3 and 7.9 EV (394-597 lux). For Distance (4 m), the acceptable range for the chart luminance was 10.5-10.7 EV (181-208 cd/m2). For Intermediate (64cm) and Near (40cm), the cceptable range for the chart luminance 10.8-11.1 EV (223-274 cd/m2). Letter-by-letter results calculated the visual performance score for each chart read. logMAR scores closer to zero, or below zero, indicate a better visual acuity. A logMAR visual performance score of 0.0 is equivalent to Snellen visual acuity of 20/20. The average score was reported for each lens.'}], 'secondaryOutcomes': [{'measure': 'CLUE Vision', 'timeFrame': '1-Week Follow-up', 'description': 'Subjective vision was assessed using the Contact Lens User Experience™ (CLUE) questionnaire. CLUE is a validated patient-reported outcomes (PRO) questionnaire to assess patient-experience attributes of soft contact lenses (comfort, vision, handling, and packaging) in a contact-lens wearing population in the US, ages 18-65. Derived CLUE scores using Item Response Theory (IRT) follow a normal distribution with a population average score of 60 (SD 20), where higher scores indicate a more favorable/positive response with a range of 0-120. The average CLUE vision score for each lens type was reported.'}]}, 'oversightModule': {'isUsExport': True, 'oversightHasDmc': False, 'isFdaRegulatedDrug': False, 'isFdaRegulatedDevice': True}, 'conditionsModule': {'conditions': ['Visual Acuity']}, 'descriptionModule': {'briefSummary': 'This is a single-masked, 2×3 crossover, randomized, dispensing clinical trial to evaluate the visual performance and subjective responses of the JJVC Investigational Contact Lens.'}, 'eligibilityModule': {'sex': 'ALL', 'stdAges': ['ADULT', 'OLDER_ADULT'], 'maximumAge': '70 Years', 'minimumAge': '40 Years', 'healthyVolunteers': True, 'eligibilityCriteria': 'Inclusion Criteria:\n\n* Potential subjects must satisfy all the following criteria to be enrolled in the study:\n\n 1. The subject must read, understand, and sign the STATEMENT OF INFORMED CONSENT and receive a fully executed copy of the form.\n 2. The subject must appear able and willing to adhere to the instructions set forth in this clinical protocol.\n 3. The subject must be at least 40 years of age and not greater than 70 years of age at the time of consent.\n 4. Subjects must own a wearable pair of spectacles if required for their distance vision.\n 5. The subject must be an adapted soft contact lens wearer in both eyes (i.e. worn lenses a minimum of 2 days per week for at least 6 hours per wear day, for 1 month or more duration).\n 6. The subject must either already be wearing a presbyopic contact lens correction (e.g., reading spectacles over contact lenses, multifocal or monovision contact lenses, etc.) or, if not respond positively to at least one symptom on the "Presbyopic Symptoms Questionnaire" (Appendix E).\n 7. The subject\'s distance spherical equivalent refraction must be in the range of +1.25 D to +3.75 D in each eye.\n 8. The subject\'s refractive cylinder must be ≤0.75 D in each eye.\n 9. The subject\'s ADD power must be in the range of +0.75 D to +2.50 D.\n 10. The subject must have distance best corrected visual acuity of 20/20-3 or better in each eye.\n\n Exclusion Criteria:\n* Potential subjects who meet any of the following criteria will be excluded from participating in the study:\n\n 1. Currently pregnant or lactating.\n 2. Any active or ongoing ocular or systemic allergies that may interfere with contact lens wear.\n 3. Any active or ongoing systemic disease, autoimmune disease, or use of medication, which may interfere with contact lens wear. This may include, but not be limited to, diabetes, hyperthyroidism, Sjögren\'s syndrome, xerophthalmia, acne rosacea, Stevens-Johnson syndrome, and immunosuppressive diseases or any infectious diseases (e.g. hepatitis, tuberculosis).\n 4. Any previous, or planned, ocular or intraocular surgery (e.g. radial keratotomy, PRK, LASIK, lid procedures, cataract surgery, retinal surgery, etc.).\n 5. A history of amblyopia, strabismus or binocular vision abnormality.\n 6. Use of any of the following medications within 1 week prior to enrollment: oral retinoid, oral tetracyclines, anticholinergics, oral phenothiazines, oral/inhaled corticosteroids. See Table 9.1 for further examples.\n 7. Use of any ocular medication, with the exception of rewetting drops.\n 8. History of herpetic keratitis.\n 9. History of irregular cornea.\n 10. History of pathological dry eye.\n 11. Participation in any contact lens or lens care product clinical trial within 30 days prior to study enrollment.\n 12. Employee or immediate family member of an employee of clinical site (e.g., Investigator, Coordinator, Technician).\n 13. Any known hypersensitivity or allergic reaction to non-preserved rewetting drop solutions or sodium fluorescein.\n 14. Clinically significant (Grade 3 or greater) corneal edema, corneal vascularization, corneal staining, tarsal abnormalities or bulbar injection, or any other corneal or ocular abnormalities which would contraindicate contact lens wear.\n 15. Entropion, ectropion, extrusions, chalazia, recurrent styes, glaucoma, history of recurrent corneal erosions.\n 16. Any current ocular infection or inflammation.\n 17. Any current ocular abnormality that may interfere with contact lens wear.'}, 'identificationModule': {'nctId': 'NCT04794751', 'briefTitle': 'Evaluation of Investigational Daily Disposable Multifocal Contact Lenses Produced With Different Manufacturing Processes', 'organization': {'class': 'INDUSTRY', 'fullName': 'Johnson & Johnson Vision Care, Inc.'}, 'officialTitle': 'Evaluation of Investigational Daily Disposable Multifocal Contact Lenses Produced With Different Manufacturing Processes', 'orgStudyIdInfo': {'id': 'CR-6418'}}, 'armsInterventionsModule': {'armGroups': [{'type': 'EXPERIMENTAL', 'label': 'senofilcon A C3/delefilcon A/delefilcon A', 'description': 'Subjects randomized to this arm will wear the senofilcon A C3 lens during period 1 and the delefilcon A lens during period 2 and period 3', 'interventionNames': ['Device: JJVC Investigational Multifocal Contact Lens', 'Device: Dailies Total 1® Multifocal Contact Lens']}, {'type': 'EXPERIMENTAL', 'label': 'delefilcon A /senofilcon A C3/senofilcon A C3', 'description': 'Subjects randomized to this arm will wear the delefilcon A lens during period 1 and the senofilcon A C3 lens during period 2 and period 3', 'interventionNames': ['Device: JJVC Investigational Multifocal Contact Lens', 'Device: Dailies Total 1® Multifocal Contact Lens']}], 'interventions': [{'name': 'JJVC Investigational Multifocal Contact Lens', 'type': 'DEVICE', 'otherNames': ['Test'], 'description': 'senofilcon A C3', 'armGroupLabels': ['delefilcon A /senofilcon A C3/senofilcon A C3', 'senofilcon A C3/delefilcon A/delefilcon A']}, {'name': 'Dailies Total 1® Multifocal Contact Lens', 'type': 'DEVICE', 'otherNames': ['Control'], 'description': 'delefilcon A', 'armGroupLabels': ['delefilcon A /senofilcon A C3/senofilcon A C3', 'senofilcon A C3/delefilcon A/delefilcon A']}]}, 'contactsLocationsModule': {'locations': [{'zip': '32256', 'city': 'Jacksonville', 'state': 'Florida', 'country': 'United States', 'facility': 'VRC-East', 'geoPoint': {'lat': 30.33218, 'lon': -81.65565}}, {'zip': '32092', 'city': 'Saint Augustine', 'state': 'Florida', 'country': 'United States', 'facility': 'St. Johns Eye Associates, PA', 'geoPoint': {'lat': 29.89469, 'lon': -81.31452}}, {'zip': '64133', 'city': 'Raytown', 'state': 'Missouri', 'country': 'United States', 'facility': 'Advanced Eyecare', 'geoPoint': {'lat': 39.00862, 'lon': -94.46356}}, {'zip': '14701', 'city': 'Jamestown', 'state': 'New York', 'country': 'United States', 'facility': 'Spectrum Eyecare', 'geoPoint': {'lat': 42.097, 'lon': -79.23533}}, {'zip': '13850', 'city': 'Vestal', 'state': 'New York', 'country': 'United States', 'facility': 'Sacco Eye Group', 'geoPoint': {'lat': 42.08507, 'lon': -76.05381}}, {'zip': '43023', 'city': 'Granville', 'state': 'Ohio', 'country': 'United States', 'facility': 'ProCare Vision Centers', 'geoPoint': {'lat': 40.06812, 'lon': -82.5196}}, {'zip': '75703', 'city': 'Tyler', 'state': 'Texas', 'country': 'United States', 'facility': 'Tyler Eye Associates', 'geoPoint': {'lat': 32.35126, 'lon': -95.30106}}], 'overallOfficials': [{'name': 'Johnson & Johnson Vision Care, Inc. Clinical Trial', 'role': 'STUDY_DIRECTOR', 'affiliation': 'Johnson & Johnson Vision Care, Inc.'}]}, 'ipdSharingStatementModule': {'url': 'http://yoda.yale.edu', 'ipdSharing': 'YES', 'description': 'Johnson \\& Johnson Medical Device Companies have an agreement with the Yale Open Data Access (YODA) to serve as the independent review panel for evaluation of requests for clinical study reports and participant level data from investigators and physicians for scientific research that will advance medical knowledge and public health. Requests for access to the study data can be submitted through the YODA Project site at http://yoda.yale.edu'}, 'sponsorCollaboratorsModule': {'leadSponsor': {'name': 'Johnson & Johnson Vision Care, Inc.', 'class': 'INDUSTRY'}, 'responsibleParty': {'type': 'SPONSOR'}}}}