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Comparison · NCT01631227-sae

Eprosartan vs Eprosartan Mesylate: 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. Eprosartan vs Eprosartan Mesylate: serious adverse events. Trial comparisons, record NCT01631227-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT01631227-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 10.009040.003080.0262wilson
Risk in group 20.02110.01020.0429wilson
Risk difference, group 1 minus group 2-0.012-0.03460.00827newcombe hybrid score
Risk ratio, group 1 over group 20.4290.1121.64log
Odds ratio, group 1 over group 20.4230.1091.65log
Number needed to treat, for one fewer participant with a serious adverse event on Eprosartan than on Eprosartan Mesylate83from 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 1EprosartanEprosartan 450 mg + Placebo Eprosartan Mesylate3332EG000
Group 2Eprosartan MesylateEprosartan Mesylate 600 mg + Placebo Eprosartan7332EG001

Harm

What it counts
Total, serious adverse events
Time frame
15 weeks (3 run-in and 12 weeks treatment)

Source ClinicalTrials.gov

Trial

Title
Comparison of the Effect of Eprosartan and Eprosartan Mesylate on Blood Pressure in Essential Hypertension
NCT number
NCT01631227
Phases
PHASE3
Conditions
Essential Hypertension
Interventions
Eprosartan, Eprosartan Mesylate, Placebo Eprosartan mesylate, Placebo Eprosartan
Lead sponsor
Abbott
Results first posted
2014-05-26

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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