Comparison · NCT00558064-sae
Telmisartan 40 mg Plus Amlodipine 5 mg Fixed-dose Combination vs Amlodipine 5 mg Monotherapy: 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 40 mg Plus Amlodipine 5 mg Fixed-dose Combination vs Amlodipine 5 mg Monotherapy: serious adverse events. Trial comparisons, record NCT00558064-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00558064-sae
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Measures6
Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.
| Measure | Value | 95% interval, lower | 95% interval, upper | Method | Note |
|---|---|---|---|---|---|
| Risk in group 1 | 0.00372 | 0.000657 | 0.0208 | wilson | |
| Risk in group 2 | 0.00763 | 0.0021 | 0.0274 | wilson | |
| Risk difference, group 1 minus group 2 | -0.00392 | -0.0239 | 0.014 | newcombe hybrid score | |
| Risk ratio, group 1 over group 2 | 0.487 | 0.0444 | 5.34 | log | |
| Odds ratio, group 1 over group 2 | 0.485 | 0.0437 | 5.38 | log | |
| Number needed to treat, for one fewer participant with a serious adverse event on Telmisartan 40 mg Plus Amlodipine 5 mg Fixed-dose Combination than on Amlodipine 5 mg Monotherapy | 255 | from the risk difference interval | the interval includes no difference |
Source ClinicalTrials.gov
Groups2
Neither group, or both, names a comparator, so the groups keep ClinicalTrials.gov's order.
| Group | Title | Description | With the outcome | Analysed | ClinicalTrials.gov code |
|---|---|---|---|---|---|
| Group 1 | Telmisartan 40 mg Plus Amlodipine 5 mg Fixed-dose Combination | T40/A5 tablet, oral, once daily in the morning | 1 | 269 | EG000 |
| Group 2 | Amlodipine 5 mg Monotherapy | A5 capsule, oral, once daily in the morning | 2 | 262 | EG001 |
Source ClinicalTrials.gov
Harm
- What it counts
- Total, serious adverse events
- Time frame
- First administration of randomised treatment to 24 hours post last dose of randomised treatment
Source ClinicalTrials.gov
Trial
- Title
- Filtered Trial for Amlodipine Non-responder
- NCT number
- NCT00558064
- Phases
- PHASE3
- Conditions
- Hypertension
- Interventions
- telmisartan+amlodipine, amlodipine
- Lead sponsor
- Boehringer Ingelheim
- Results first posted
- 2010-02-01
- Results on ClinicalTrials.gov
- https://clinicaltrials.gov/study/NCT00558064?tab=results
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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