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5ARI Users vs Non 5ARI Users: Suicide Attempt (Based on Administrative Data Elements From National Ambulatory Care Reporting System, and Ontario Regional Mental Health Database)

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

Measures 6

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

MeasureValue95% interval, lower95% interval, upperMethodNoteSource
Risk in group 10.001810.001560.00211wilsonClinicalTrials.gov
Risk in group 20.001390.001170.00166wilsonClinicalTrials.gov
Risk difference, group 1 minus group 20.0004180.00005470.000786newcombe hybrid scoreClinicalTrials.gov
Risk ratio, group 1 over group 21.31.031.63logClinicalTrials.gov
Odds ratio, group 1 over group 21.31.031.63logClinicalTrials.gov
Number needed to treat, for one more participant with the outcome on 5ARI Users than on Non 5ARI Users2,3901,27018,300from the risk difference intervalClinicalTrials.gov

Groups 2

Neither group, or both, names a comparator, so the groups keep ClinicalTrials.gov's order.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov codeSource
Group 15ARI Users5ARI: Exposure to finasteride/dutasteride16993,197OG000ClinicalTrials.gov
Group 2Non 5ARI Users13093,197OG001ClinicalTrials.gov

Outcome 5

FieldValueSource
TypeSECONDARYClinicalTrials.gov
TitleSuicide Attempt (Based on Administrative Data Elements From National Ambulatory Care Reporting System, and Ontario Regional Mental Health Database)ClinicalTrials.gov
Description
1. NACRS: presentation to the emergency room: ICD 10 codes X60-X84 (intentional self harm).~2. OMHRS: admission with suicide ideation.~i. Self injury attempts: D1A or selfinjury\_attempt=3, 4, 5, or 6 ii. Self injury intent: D1B or selfinjury\_intent=1 iii. Self injury considered: D1C or selfinjury\_cons=3, 4, 5 or 6 iv. Self injury plan: D1DB or suicide\_plan=1
ClinicalTrials.gov
Time frameThrough study completition, an average of 18 months.ClinicalTrials.gov
PopulationClinicalTrials.gov

Trial 8

FieldValueSource
Title5 Alpha Reductase Inhibitors And The Risk Of Suicide And DepressionClinicalTrials.gov
NCT numberNCT02876757ClinicalTrials.gov
PhasesClinicalTrials.gov
ConditionsBPH, Depression, SuicideClinicalTrials.gov
Interventions5ARIClinicalTrials.gov
Lead sponsorLondon Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph'sClinicalTrials.gov
Results first posted2018-02-05ClinicalTrials.gov
Results on ClinicalTrials.govhttps://clinicaltrials.gov/study/NCT02876757?tab=resultsClinicalTrials.gov

Source 4

FieldValueSource
Releasetrial-comparisons-2026-03-23-0.1.0ClinicalTrials.gov
Release manifest SHA-256f66225897fbf258b57ea10bdacfd0347d3cdfda93f7f5685234b7e06ea36fa57ClinicalTrials.gov
AACT copy2026-03-23ClinicalTrials.gov
Tables readoutcome_counts.parquet, outcome_measurements.parquet, outcomes.parquet, reported_event_totals.parquet, reported_events.parquet, result_groups.parquet, studies.parquet, ctgov_trial.parquetClinicalTrials.gov

The same record as JSON

Release trial-comparisons-2026-03-23-0.1.0

ClinicalTrials.gov's posted results, through CTTI's AACT: ClinicalTrials.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.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.

ClinicalTrials.gov: none 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.