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Trial · NCT03863080

Adverse events156

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

TypeEventOrgan systemGroupAffectedAt riskEvents
otherGingival painGastrointestinal disordersDouble-blind Treatment Period: Placebo06
otherGingival painGastrointestinal disordersDouble-blind Treatment Period: RVT-1401 340 mg/Week05
otherGingival painGastrointestinal disordersDouble-blind Treatment Period: RVT-1401 680 mg/Week16
otherGingival painGastrointestinal disordersOpen-label Extension Period: RVT-1401 340 mg Biweekly015
otherAnal incontinenceGastrointestinal disordersDouble-blind Treatment Period: Placebo16
otherAnal incontinenceGastrointestinal disordersDouble-blind Treatment Period: RVT-1401 340 mg/Week05
otherAnal incontinenceGastrointestinal disordersDouble-blind Treatment Period: RVT-1401 680 mg/Week06
otherAnal incontinenceGastrointestinal disordersOpen-label Extension Period: RVT-1401 340 mg Biweekly015
otherConstipationGastrointestinal disordersDouble-blind Treatment Period: Placebo16
otherConstipationGastrointestinal disordersDouble-blind Treatment Period: RVT-1401 340 mg/Week05
otherConstipationGastrointestinal disordersDouble-blind Treatment Period: RVT-1401 680 mg/Week06
otherConstipationGastrointestinal disordersOpen-label Extension Period: RVT-1401 340 mg Biweekly015
otherDiarrhoeaGastrointestinal disordersDouble-blind Treatment Period: Placebo16
otherDiarrhoeaGastrointestinal disordersDouble-blind Treatment Period: RVT-1401 340 mg/Week05
otherDiarrhoeaGastrointestinal disordersDouble-blind Treatment Period: RVT-1401 680 mg/Week06
otherDiarrhoeaGastrointestinal disordersOpen-label Extension Period: RVT-1401 340 mg Biweekly015
otherNauseaGastrointestinal disordersDouble-blind Treatment Period: Placebo06
otherNauseaGastrointestinal disordersDouble-blind Treatment Period: RVT-1401 340 mg/Week05
otherNauseaGastrointestinal disordersDouble-blind Treatment Period: RVT-1401 680 mg/Week06
otherNauseaGastrointestinal disordersOpen-label Extension Period: RVT-1401 340 mg Biweekly115

Source ClinicalTrials.govtrials-2026-11-12-0.4.0

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNone 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.

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GET https://conductscience.org/api/trials/v1/NCT03863080/events