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TICAGRELOR vs PLACEBO: Bleeding Event That Fulfils Serious Adverse Event Criteria and is Categorised as GUSTO Moderate/Severe

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 10.006520.004710.00901wilsonClinicalTrials.gov
Risk in group 20.0020.001120.00358wilsonClinicalTrials.gov
Risk difference, group 1 minus group 20.004520.002120.00716newcombe hybrid scoreClinicalTrials.gov
Risk ratio, group 1 over group 23.251.666.39logClinicalTrials.gov
Odds ratio, group 1 over group 23.271.666.43logClinicalTrials.gov
Number needed to treat, for one more participant with the outcome on TICAGRELOR than on PLACEBO221140473from the risk difference intervalClinicalTrials.gov

Groups 2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov codeSource
Group 1TICAGRELORTicagrelor 180 mg day 1, followed by 90 mg twice daily day 2-30365,523OG000ClinicalTrials.gov
Group 2PLACEBOPlacebo 180 mg day 1, followed by 90 mg twice daily day 2-30115,493OG001ClinicalTrials.gov

Outcome 5

FieldValueSource
TypeOTHER_PRE_SPECIFIEDClinicalTrials.gov
TitleBleeding Event That Fulfils Serious Adverse Event Criteria and is Categorised as GUSTO Moderate/SevereClinicalTrials.gov
Description
Participants with bleeding event that fulfils serious adverse event criteria and is categorised as GUSTO Moderate/Severe. GUSTO is a bleeding scale (GUSTO = Global Utilization of Streptokinase and Tissue plasminogen activator for Occluded coronary arteries). GUSTO Severe bleeding is defined as any of the following: (1) fatal bleeding, (2) intracranial bleeding, or (3) bleeding that caused haemodynamic compromise requiring intervention. GUSTO Moderate bleeding is a bleeding requiring transfusion of whole blood or packed red blood cells without haemodynamic compromise
ClinicalTrials.gov
Time frameFrom randomisation (day 1) to visit 3 (day 30-34)ClinicalTrials.gov
PopulationFull analysis set including all randomised patientsClinicalTrials.gov

Trial 8

FieldValueSource
TitleTHALES - Acute STroke or Transient IscHaemic Attack Treated With TicAgreLor and ASA for PrEvention of Stroke and DeathClinicalTrials.gov
NCT numberNCT03354429ClinicalTrials.gov
PhasesPHASE3ClinicalTrials.gov
ConditionsAcute Ischaemic Stroke, Transient Ischaemic AttackClinicalTrials.gov
InterventionsTicagrelor, PlaceboClinicalTrials.gov
Lead sponsorAstraZenecaClinicalTrials.gov
Results first posted2020-12-22ClinicalTrials.gov
Results on ClinicalTrials.govhttps://clinicaltrials.gov/study/NCT03354429?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.