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Trial · NCT01469156

Outcomes13

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYIncidence and Severity of Ocular and Systemic Adverse Events Will be Compared Between the 2.0mg or 1.0mg (HIGH DOSE) and 0.5 mg Groups.2 yearsAdverse eventsNUMBER
SECONDARYMean Best Corrected Visual Acuity Letter Change at 4 Meters Between Baseline and 12 Months12 monthsRandomized in a 3:1 ratio - number in participant flow is 20lettersMEAN
SECONDARYChange in Mean Central Foveal Thickness From Baseline12 MonthsRandomized in a 3:1 ratioumMEAN
SECONDARYMean Change From Baseline in Total Area of FA CNV Leakage Over 12 Months12 MonthsRandomized in a 3:1 ratiomm^2MEAN
SECONDARYNumber of Participants at Month 3 With Best Corrected Visual Acuity Gain of 5, 10, and 15 or More Letters3 MonthsRandomized in a 3:1 ratio - number in participant flow is 20ParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYNumber of Participants at Month 6 With Best Corrected Visual Acuity Gain of 5, 10, and 15 or More Letters6 monthsRandomized in a 3:1 ratio - number in participant flow is 20ParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYNumber of Participants at Month 9 With Best Corrected Visual Acuity Gain of 5, 10, and 15 or More Letters9 MonthsRandomized in a 3:1 ratio - number in participant flow is 20ParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYNumber of Participants at Month 12 With Best Corrected Visual Acuity Gain of 5, 10, and 15 or More Letters12 MonthsRandomized in a 3:1 ratio - number in participant flow is 20ParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYMean Change Best Corrected Visual Acuity at 4 Meters at Baseline, Month 3, Month 6, Month 9, and Month 1212 monthsRandomized in a 3:1 ratio - number in participant flow is 20lettersMEAN
SECONDARYNumber of Participants at Month 3 With Best Corrected Visual Acuity Loss at 4 Meters of 5, 10 and 15 or More Letters3 monthsRandomized in a 3:1 ratio - number in participant flow is 20ParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYNumber of Participants at Month 6 With Best Corrected Visual Acuity Loss at 4 Meters of 5, 10 and 15 or More Letters6 monthsRandomized in a 3:1 ratio - number in participant flow is 20ParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYNumber of Participants at Month 9 With Best Corrected Visual Acuity Loss at 4 Meters of 5, 10 and 15 or More Letters9 monthsRandomized in a 3:1 ratio - number in participant flow is 20ParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYNumber of Participants at Month 12 With Best Corrected Visual Acuity Loss at 4 Meters of 5, 10 and 15 or More Letters12 monthsRandomized in a 3:1 ratio - number in participant flow is 20ParticipantsCOUNT_OF_PARTICIPANTS

Source ClinicalTrials.govtrials-2026-11-12-0.5.0

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

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GET https://conductscience.org/api/trials/v1/NCT01469156/outcomes