Adverse event totals15

The totals the trial posted for each group.

1 to 15 of 15

Total	Group	Affected	At risk
Total, all-cause mortality	Vitamin D
Total, all-cause mortality	Placebo- Vitamin D
Total, all-cause mortality	Probenecid
Total, all-cause mortality	Allopurinol
Total, all-cause mortality	Placebo- Uric Acid
Total, other adverse events	Vitamin D	5	43
Total, other adverse events	Placebo- Vitamin D	6	45
Total, other adverse events	Probenecid	16	46
Total, other adverse events	Allopurinol	36	48
Total, other adverse events	Placebo- Uric Acid	25	51
Total, serious adverse events	Vitamin D	0	43
Total, serious adverse events	Placebo- Vitamin D	0	45
Total, serious adverse events	Probenecid	4	46
Total, serious adverse events	Allopurinol	6	48
Total, serious adverse events	Placebo- Uric Acid	2	51

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

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

Twenty rows a page, as JSON. No key.

GET https://conductscience.org/api/trials/v1/NCT01320722/event-totals