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Trial · NCT02507011

Adverse events12

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

TypeEventOrgan systemGroupAffectedAt riskEvents
otherFatigueGeneral disordersCarvedilol121
otherFatigueGeneral disordersPlacebo121
otherHypotensionGeneral disordersCarvedilol121
otherHypotensionGeneral disordersPlacebo020
otherFluid RetentionGeneral disordersCarvedilol121
otherFluid RetentionGeneral disordersPlacebo121
otherConstipationGastrointestinal disordersCarvedilol020
otherConstipationGastrointestinal disordersPlacebo122
otherGastroenteritisGastrointestinal disordersCarvedilol020
otherGastroenteritisGastrointestinal disordersPlacebo122
seriousHF Exaceberation/Electrolyte ImbalanceGeneral disordersCarvedilol123
seriousHF Exaceberation/Electrolyte ImbalanceGeneral disordersPlacebo121

Source ClinicalTrials.govtrials-2026-11-12-0.5.0

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
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
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this list from software.

Twenty rows a page, as JSON. No key.

GET https://conductscience.org/api/trials/v1/NCT02507011/events