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Comparison · NCT05039086-deaths

PDE5 Inhibitors vs Endothelin Receptor Antagonists: deaths from any cause

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. PDE5 Inhibitors vs Endothelin Receptor Antagonists: deaths from any cause. Trial comparisons, record NCT05039086-deaths. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT05039086-deaths

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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 10.1130.1020.125wilson
Risk in group 20.1410.1290.154wilson
Risk difference, group 1 minus group 2-0.0277-0.0449-0.0105newcombe hybrid score
Risk ratio, group 1 over group 20.8030.7010.921log
Odds ratio, group 1 over group 20.7780.6660.909log
Number needed to treat, for one fewer death from any cause on PDE5 Inhibitors than on Endothelin Receptor Antagonists36.122.395from the risk difference interval

Groups2

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

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1PDE5 InhibitorsExposure group~PDE5 inhibitor: PDE5 inhibitors (sildenafil, tadalafil) claim is used as the exposure group.3272,888EG000
Group 2Endothelin Receptor AntagonistsReference group~Endothelin Receptor Antagonists: Endothelin receptor antagonists (bosentan, ambrisentan, macitentan) claim is used as the reference group.4072,888EG001

Harm

What it counts
Total, all-cause mortality
Time frame

Source ClinicalTrials.gov

Trial

Title
Data Analysis for Drug Repurposing for Effective Alzheimer's Medicines (DREAM) - PDE5
NCT number
NCT05039086
Phases
Conditions
Pulmonary Arterial Hypertension
Interventions
PDE5 inhibitor, Endothelin Receptor Antagonists
Lead sponsor
Brigham and Women's Hospital
Results first posted
2024-02-20

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.govNone 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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