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Ticagrelor 90 mg vs ASA 100 mg: Number of Participants With Disabling Stroke

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 10.0420.03750.0472wilsonClinicalTrials.gov
Risk in group 20.04640.04160.0518wilsonClinicalTrials.gov
Risk difference, group 1 minus group 2-0.00441-0.01140.00262newcombe hybrid scoreClinicalTrials.gov
Risk ratio, group 1 over group 20.9050.7721.06logClinicalTrials.gov
Odds ratio, group 1 over group 20.9010.7631.06logClinicalTrials.gov
Number needed to treat, for one fewer participant with the outcome on Ticagrelor 90 mg than on ASA 100 mg227from 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 1Ticagrelor 90 mgTicagrelor 90 mg twice daily (BD)2776,589OG000ClinicalTrials.gov
Group 2ASA 100 mgASA 100 mg once daily (OD)3076,610OG001ClinicalTrials.gov

Outcome 5

FieldValueSource
TypeSECONDARYClinicalTrials.gov
TitleNumber of Participants With Disabling StrokeClinicalTrials.gov
DescriptionParticipants with disabling stroke. If no event, censoring at the minimum of (last date of event assessment, date of death, end of treatment date, day 97).ClinicalTrials.gov
Time frameFrom randomization up to 97 daysClinicalTrials.gov
PopulationThe population was the full analysis set, which included all randomized patients.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.