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Comparison · NCT01585441-c80d910d

Finasteride 5 mg vs Placebo: Number of Participants Presenting No Change in Fluid Leakage at the Safety Visit Compared to Baseline

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

2 sourcestrial-comparisons-2026-03-23-0.1.0

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ConductScience Library. Finasteride 5 mg vs Placebo: Number of Participants Presenting No Change in Fluid Leakage at the Safety Visit Compared to Baseline. Trial comparisons, record NCT01585441-c80d910d. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT01585441-c80d910d

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Measures6

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

MeasureValue95% interval, lower95% interval, upperMethodNote
Risk in group 10.6670.2080.939wilson
Risk in group 210.3421wilson
Risk difference, group 1 minus group 2-0.333-0.7920.378newcombe hybrid score
Risk ratio, group 1 over group 20.6670.31.48log
Odds ratio, group 1 over group 2loga cell of the two-by-two table is zero
Number needed to treat, for one fewer participant with the outcome on Finasteride 5 mg than on Placebo3from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Finasteride 5 mg
Participants randomly assigned to the finasteride 5 mg arm were instructed to take one capsule daily for three months.~Finasteride: Finasteride is available as white, round 5 mg tablets. During the masked period, the tablets are re-formulated in capsules with inactive ingredients. The re-formulated finasteride capsules are indistinguishable from the placebo capsules.
23OG000
Group 2PlaceboParticipants randomly assigned to the placebo arm will instructed to take one capsule daily for three months.~Placebo: Capsule with no active ingredients to mimic finasteride22OG001

Outcome

Type
SECONDARY
Title
Number of Participants Presenting No Change in Fluid Leakage at the Safety Visit Compared to Baseline
Description
Changes in leakage as observed on fluorescein angiography (FA)
Time frame
Final Study Visit
Population

Source ClinicalTrials.gov

Trial

Title
Finasteride for Chronic Central Serous Chorioretinopathy
NCT number
NCT01585441
Phases
PHASE2
Conditions
Retinal Disease
Interventions
Finasteride, Placebo
Lead sponsor
National Eye Institute (NEI)
Results first posted
2014-12-04

Source ClinicalTrials.gov

Source

Release
trial-comparisons-2026-03-23-0.1.0
Release manifest SHA-256
f66225897fbf258b57ea10bdacfd0347d3cdfda93f7f5685234b7e06ea36fa57
AACT copy
2026-03-23
Tables read
outcome_counts.parquet, outcome_measurements.parquet, outcomes.parquet, reported_event_totals.parquet, reported_events.parquet, result_groups.parquet, studies.parquet, ctgov_trial.parquet

Source ClinicalTrials.gov

Sources 2

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
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

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions. The measures are ConductScience's calculation from them.

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