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Trial · NCT01228903

Adverse events12

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

TypeEventOrgan systemGroupAffectedAt riskEvents
othergoutMusculoskeletal and connective tissue disordersControl141
othergoutMusculoskeletal and connective tissue disordersAllopurinol139
otherGI discomfortGastrointestinal disordersControl241
otherGI discomfortGastrointestinal disordersAllopurinol239
otherrashSkin and subcutaneous tissue disordersControl241
otherrashSkin and subcutaneous tissue disordersAllopurinol039
otherAbnormal Liver Function TestsHepatobiliary disordersControl241
otherAbnormal Liver Function TestsHepatobiliary disordersAllopurinol039
otherThrombocytopeniaBlood and lymphatic system disordersControl241
otherThrombocytopeniaBlood and lymphatic system disordersAllopurinol139
seriousDeathCardiac disordersControl0410
seriousDeathCardiac disordersAllopurinol1391

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

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GET https://conductscience.org/api/trials/v1/NCT01228903/events