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ASA 100mg vs Ticagrelor 90mg: serious adverse events

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 10.0810.07460.0878wilsonClinicalTrials.gov
Risk in group 20.08120.07490.0881wilsonClinicalTrials.gov
Risk difference, group 1 minus group 2-0.000243-0.009590.00911newcombe hybrid scoreClinicalTrials.gov
Risk ratio, group 1 over group 20.9970.8891.12logClinicalTrials.gov
Odds ratio, group 1 over group 20.9970.8791.13logClinicalTrials.gov
Number needed to treat, for one fewer participant with a serious adverse event on ASA 100mg than on Ticagrelor 90mg4,110from the risk difference intervalthe interval includes no differenceClinicalTrials.gov

Groups 2

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

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov codeSource
Group 1ASA 100mgASA 100 mg once daily (OD)5336,581EG000ClinicalTrials.gov
Group 2Ticagrelor 90mgTicagrelor 90 mg twice daily (BD)5326,549EG001ClinicalTrials.gov

Harm 2

FieldValueSource
What it countsTotal, serious adverse eventsClinicalTrials.gov
Time frameOn or after the date of first dose and up to and including 7 days following the date of last dose of study medication. 97 days if the participant completed treatment according to the study plan.ClinicalTrials.gov

Trial 8

FieldValueSource
Title[SOCRATES -Acute Stroke Or Transient IsChaemic Attack TReated With Aspirin or Ticagrelor and Patient OutcomES]ClinicalTrials.gov
NCT numberNCT01994720ClinicalTrials.gov
PhasesPHASE3ClinicalTrials.gov
ConditionsAcute Ischaemic Stroke, Transient Ischaemic AttackClinicalTrials.gov
Interventionsticagrelor, Acetylsalicylic acid (ASA)ClinicalTrials.gov
Lead sponsorAstraZenecaClinicalTrials.gov
Results first posted2017-06-12ClinicalTrials.gov
Results on ClinicalTrials.govhttps://clinicaltrials.gov/study/NCT01994720?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.