ConductScience.org, home

Library / Trial comparisons

Placebo + Ticagrelor vs Aspirin + Ticagrelor: Number of Participants With BARC Type 2, 3, or 5

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 10.03970.03370.0466wilsonClinicalTrials.gov
Risk in group 20.07010.06220.079wilsonClinicalTrials.gov
Risk difference, group 1 minus group 2-0.0305-0.0411-0.02newcombe hybrid scoreClinicalTrials.gov
Risk ratio, group 1 over group 20.5650.4620.691logClinicalTrials.gov
Odds ratio, group 1 over group 20.5470.4430.677logClinicalTrials.gov
Number needed to treat, for one fewer participant with the outcome on Placebo + Ticagrelor than on Aspirin + Ticagrelor32.824.350.1from 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 1Placebo + Ticagrelorplacebo pill daily p.o. for 12 months - match for enteric coated aspirin 81mg-100mg and ticagrelor 90mg tablet bid for 12 months1413,555OG000ClinicalTrials.gov
Group 2Aspirin + Ticagrelorenteric coated aspirin 81mg-100mg daily p.o. for 12 months and ticagrelor 90mg tablet bid for 12 months2503,564OG001ClinicalTrials.gov

Outcome 5

FieldValueSource
TypePRIMARYClinicalTrials.gov
TitleNumber of Participants With BARC Type 2, 3, or 5ClinicalTrials.gov
Description
Number of participants with first occurrence of clinically relevant bleeding episode, defined as Bleeding Academic Research Consortium (BARC) Types 2, 3 or 5 bleeding. BARC bleeding types range from 0 (no bleeding) to 5 (fatal bleeding).
ClinicalTrials.gov
Time frame12 months after randomizationClinicalTrials.gov
PopulationData for the intention-to-treat populationClinicalTrials.gov

Trial 8

FieldValueSource
TitleTicagrelor With Aspirin or Alone in High-Risk Patients After Coronary InterventionClinicalTrials.gov
NCT numberNCT02270242ClinicalTrials.gov
PhasesPHASE4ClinicalTrials.gov
ConditionsCardiovascular Disease, Interventional CardiologyClinicalTrials.gov
InterventionsAspirin, Placebo, ticagrelorClinicalTrials.gov
Lead sponsorIcahn School of Medicine at Mount SinaiClinicalTrials.gov
Results first posted2020-08-19ClinicalTrials.gov
Results on ClinicalTrials.govhttps://clinicaltrials.gov/study/NCT02270242?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.