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Telmisartan (TRANSCEND) vs Placebo (TRANSCEND): TRANSCEND. Composite Endpoint of Cardiovascular Death, Non-fatal Myocardial Infarction and Non-fatal 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 10.130.1180.143wilsonClinicalTrials.gov
Risk in group 20.1480.1360.161wilsonClinicalTrials.gov
Risk difference, group 1 minus group 2-0.0181-0.0357-0.000431newcombe hybrid scoreClinicalTrials.gov
Risk ratio, group 1 over group 20.8780.7730.997logClinicalTrials.gov
Odds ratio, group 1 over group 20.860.7420.996logClinicalTrials.gov
Number needed to treat, for one fewer participant with the outcome on Telmisartan (TRANSCEND) than on Placebo (TRANSCEND)55.4282,320from the risk difference intervalClinicalTrials.gov

Groups 2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov codeSource
Group 1Telmisartan (TRANSCEND)Telmisartan 80mg tablet, one tablet administered once daily in the morning.3842,954OG000ClinicalTrials.gov
Group 2Placebo (TRANSCEND)Telmisartan 80mg placebo tablet, one tablet administered once daily in the morning.4402,972OG001ClinicalTrials.gov

Outcome 5

FieldValueSource
TypeSECONDARYClinicalTrials.gov
TitleTRANSCEND. Composite Endpoint of Cardiovascular Death, Non-fatal Myocardial Infarction and Non-fatal StrokeClinicalTrials.gov
Description
Telmisartan Randomized Assessment Study in Angiotension Converting Enzyme inhibitor intolerant subjects with cardiovascular disease (TRANSCEND). Time to first event analysis of the following defined endpoints, Cardiovascular Death, Non-fatal myocardial infarction, non-fatal stroke and hospitalization for congestive heart failure.
ClinicalTrials.gov
Time frame56 monthsClinicalTrials.gov
PopulationFAS of the TRANSCEND trialClinicalTrials.gov

Trial 8

FieldValueSource
Title
Effectiveness and Safety of Ramipril Alone Compared With Telmisartan Alone and in Combination With Ramipril in Patients at High Risk for Cardiovascular Events. Patients Intolerant to Ramipril Were Entered in TRANSCEND, Telmisartan Compared to Placebo.
ClinicalTrials.gov
NCT numberNCT00153101ClinicalTrials.gov
PhasesPHASE4ClinicalTrials.gov
ConditionsCardiovascular DiseasesClinicalTrials.gov
InterventionsTelmisartan, Combination of Telmisartan and Ramipril, RamiprilClinicalTrials.gov
Lead sponsorBoehringer IngelheimClinicalTrials.gov
Results first posted2009-08-25ClinicalTrials.gov
Results on ClinicalTrials.govhttps://clinicaltrials.gov/study/NCT00153101?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.