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Comparison · NCT00614380-sae

Telmisartan 40mg and Amlodipine 5mg vs Telmisartan 80mg and Amlodipine 5mg: serious adverse events

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

2 sourcestrial-comparisons-2026-03-23-0.1.0

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ConductScience Library. Telmisartan 40mg and Amlodipine 5mg vs Telmisartan 80mg and Amlodipine 5mg: serious adverse events. Trial comparisons, record NCT00614380-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00614380-sae

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Measures6

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

MeasureValue95% interval, lower95% interval, upperMethodNote
Risk in group 10.02250.01490.0339wilson
Risk in group 20.01510.006940.0326wilson
Risk difference, group 1 minus group 20.00743-0.01160.0214newcombe hybrid score
Risk ratio, group 1 over group 21.490.6093.65log
Odds ratio, group 1 over group 21.50.6053.73log
Number needed to harm, for one more participant with a serious adverse event on Telmisartan 40mg and Amlodipine 5mg than on Telmisartan 80mg and Amlodipine 5mg135from the risk difference intervalthe interval includes no difference

Groups2

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

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Telmisartan 40mg and Amlodipine 5mg22976EG000
Group 2Telmisartan 80mg and Amlodipine 5mg6397EG001

Harm

What it counts
Total, serious adverse events
Time frame
From day of first dose until one day after last dose

Source ClinicalTrials.gov

Trial

Title
Open Label Study Telmisartan and Amlodipine in Hypertension
NCT number
NCT00614380
Phases
PHASE3
Conditions
Hypertension
Interventions
telmisartan/amlodipine 40/5 mg fixed combination, telmisartan/amlodipine 80/5 mg fixed combination
Lead sponsor
Boehringer Ingelheim
Results first posted
2010-01-18

Source ClinicalTrials.gov

Source

Release
trial-comparisons-2026-03-23-0.1.0
Release manifest SHA-256
f66225897fbf258b57ea10bdacfd0347d3cdfda93f7f5685234b7e06ea36fa57
AACT copy
2026-03-23
Tables read
outcome_counts.parquet, outcome_measurements.parquet, outcomes.parquet, reported_event_totals.parquet, reported_events.parquet, result_groups.parquet, studies.parquet, ctgov_trial.parquet

Source ClinicalTrials.gov

Sources 2

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.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.govnone 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.

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