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Trial · NCT05856760

Adverse events11

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

TypeEventOrgan systemGroupAffectedAt riskEvents
otherHypotensionVascular disordersSparsentan748
otherHeadacheNervous system disordersSparsentan448
otherOedemaGeneral disordersSparsentan448
otherOedema peripheralGeneral disordersSparsentan448
otherUpper respiratory tract infectionInfections and infestationsSparsentan448
otherDizzinessNervous system disordersSparsentan348
seriousOsteoarthritisMusculoskeletal and connective tissue disordersSparsentan1481
seriousCerebrovascular eventNervous system disordersSparsentan1481
seriousAcute kidney injuryRenal and urinary disordersSparsentan1481
seriousDeep vein thrombosisVascular disordersSparsentan1481
seriousChemical burnInjury, poisoning and procedural complicationsSparsentan1481

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.

For software

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Twenty rows a page, as JSON. No key.

GET https://conductscience.org/api/trials/v1/NCT05856760/events