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Trial · NCT01780935

Outcomes13

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

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYAverage Best-corrected Visual Acuity (BCVA) (Letters) Change up to Month 12up to Month 12Full Analysis Set (FAS) includes all randomized patientsLetters correctly readMEAN
SECONDARYChange From Baseline in Visual Acuity (Letters) of the Study Eye up to Month 12up to Month 12Full Analysis Set (FAS) includes all randomized patientsletters correctly readMEAN
SECONDARYGain of Equal or More Than 1, 5, 10, or 15 Letters in Visual Acuity of the Study Eye From Baseline, at Month 12 and 24Baseline to Month 12 and 24Early termination of the study, therefore the 12-month cutoff date was not reached and the related analysis was not performed
SECONDARYLoss of Less Than 5, 10, and 15 Letters in Visual Acuity in the Study Eye From Baseline, at Month 12 and 24Baseline to Month 12 and 24Early termination of the study, therefore the 12-month cutoff date was not reached and the related analysis was not performed
SECONDARYVisual Acuity of 73 Letters or More in the Study Eye at Month 12 and 24Month 12 and 24Early termination of the study, therefore the 12-month cutoff date was not reached and the related analysis was not performed
SECONDARYAverage Visual Acuity Change From Month 3 to Month 4 Through Month 24 in the Study EyeMonth 3 to Month 24Early termination of the study, therefore the 12-month cutoff date was not reached and the related analysis was not performed
SECONDARYAverage Visual Acuity Change From Baseline to Month 1 Through Month 12 and 24 in the Study EyeBaseline to Month 12 and 24Early termination of the study, therefore the 12-month cutoff date was not reached and the related analysis was not performed
SECONDARYChange From Baseline in Central Sub-Field Thickness (CSFT) and Central Sub-Field Volume (CSFV) of the Study Eye Over TimeBaseline to Month 12 and 24Early termination of the study, therefore the 12-month cutoff date was not reached and the related analysis was not performed
SECONDARYDry Retina in the Study Eye on OCT at Month 12 and 24Month 12 and 24Early termination of the study, therefore the 12-month cutoff date was not reached and the related analysis was not performed
SECONDARYChange From Baseline in Lesion Size and Morphology Based on Fluorescein Angiography at Month 12 and 24Baseline to Month 12 and 24Early termination of the study, therefore the 12-month cutoff date was not reached and the related analysis was not performed
SECONDARYTreatment Patterns Over Time in Both Treatment ArmsBaseline to Month 12 and 24Early termination of the study, therefore the 12-month cutoff date was not reached and the related analysis was not performed
SECONDARYChange From Baseline in the National Eye Institute Visual Functioning Questionnaire (NEI-VFQ-25) Scores Over TimeBaseline to Month 12 and 24Early termination of the study, therefore the 12-month cutoff date was not reached and the related analysis was not performed
SECONDARYFrequency and Severity of Ocular and Non-ocular Adverse Events Over TimeScreening to Month 12 and 24Early termination of the study, therefore the 12-month cutoff date was not reached and the related analysis was not performed

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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