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Vitamins vs Placebo: serious adverse events

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

Measures 6

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

MeasureValue95% interval, lower95% interval, upperMethodNoteSource
Risk in group 10.02120.01760.0256wilsonClinicalTrials.gov
Risk in group 20.03420.02950.0395wilsonClinicalTrials.gov
Risk difference, group 1 minus group 2-0.0129-0.0194-0.00656newcombe hybrid scoreClinicalTrials.gov
Risk ratio, group 1 over group 20.6220.490.788logClinicalTrials.gov
Odds ratio, group 1 over group 20.6130.4810.783logClinicalTrials.gov
Number needed to treat, for one fewer participant with a serious adverse event on Vitamins than on Placebo77.451.6152from the risk difference intervalClinicalTrials.gov

Groups 2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov codeSource
Group 1VitaminsVitamins C \& E1085,087EG000ClinicalTrials.gov
Group 2PlaceboMineral Oil, Hydrogenated Vegetable Oil, Lecithin, Yellow wax, Soft Gelatin Shell1735,065EG001ClinicalTrials.gov

Harm 2

FieldValueSource
What it countsTotal, serious adverse eventsClinicalTrials.gov
Time frame
Adverse event data was collected beginning with enrollment (between 9 weeks 0 days gestation and 16 weeks 6 days gestation) through the duration of the pregnancy, delivery, and hospital discharge for the mother and baby. This time period varies by participant and may cover anywhere from 9 weeks gestation to 42 weeks gestation.
ClinicalTrials.gov

Trial 8

FieldValueSource
TitleCombined Antioxidant and Preeclampsia Prediction Studies (CAPPS)ClinicalTrials.gov
NCT numberNCT00135707ClinicalTrials.gov
PhasesPHASE3ClinicalTrials.gov
ConditionsPreeclampsiaClinicalTrials.gov
InterventionsDietary Supplement/Vitamins, Placebo for Vitamin C and Vitamin EClinicalTrials.gov
Lead sponsorThe George Washington University Biostatistics CenterClinicalTrials.gov
Results first posted2018-11-20ClinicalTrials.gov
Results on ClinicalTrials.govhttps://clinicaltrials.gov/study/NCT00135707?tab=resultsClinicalTrials.gov

Source 4

FieldValueSource
Releasetrial-comparisons-2026-03-23-0.1.0ClinicalTrials.gov
Release manifest SHA-256f66225897fbf258b57ea10bdacfd0347d3cdfda93f7f5685234b7e06ea36fa57ClinicalTrials.gov
AACT copy2026-03-23ClinicalTrials.gov
Tables readoutcome_counts.parquet, outcome_measurements.parquet, outcomes.parquet, reported_event_totals.parquet, reported_events.parquet, result_groups.parquet, studies.parquet, ctgov_trial.parquetClinicalTrials.gov

The same record as JSON

Release trial-comparisons-2026-03-23-0.1.0

ClinicalTrials.gov's posted results, through CTTI's AACT: ClinicalTrials.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.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions. The measures are ConductScience's calculation from them.

ClinicalTrials.gov: none stated ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions. The measures are ConductScience's calculation from them.