Comparison · NCT01857310-aa874ba5
Folic Acid and Zinc Supplementation vs Placebo: Severe Maternal Morbidity
Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.
2 sourcestrial-comparisons-2026-03-23-0.1.0
Cite this record
ConductScience Library. Folic Acid and Zinc Supplementation vs Placebo: Severe Maternal Morbidity. Trial comparisons, record NCT01857310-aa874ba5. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT01857310-aa874ba5
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Measures6
Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.
| Measure | Value | 95% interval, lower | 95% interval, upper | Method | Note |
|---|---|---|---|---|---|
| Risk in group 1 | 0.0127 | 0.00769 | 0.0208 | wilson | |
| Risk in group 2 | 0.00844 | 0.00459 | 0.0155 | wilson | |
| Risk difference, group 1 minus group 2 | 0.00422 | -0.00439 | 0.0132 | newcombe hybrid score | |
| Risk ratio, group 1 over group 2 | 1.5 | 0.677 | 3.33 | log | |
| Odds ratio, group 1 over group 2 | 1.51 | 0.674 | 3.37 | log | |
| Number needed to treat, for one more participant with the outcome on Folic Acid and Zinc Supplementation than on Placebo | 237 | from the risk difference interval | the interval includes no difference |
Source ClinicalTrials.gov
Groups2
Group 2 names the comparator: placebo.
| Group | Title | Description | With the outcome | Analysed | ClinicalTrials.gov code |
|---|---|---|---|---|---|
| Group 1 | Folic Acid and Zinc Supplementation | 5 mg folic acid and 30 mg elemental zinc, taken orally, daily for 6 months.~5 mg folic acid and 30 mg elemental zinc | 15 | 1,185 | OG000 |
| Group 2 | Placebo | Matching placebo, taken orally daily for 6 months.~Placebo Comparator: Placebo | 10 | 1,185 | OG001 |
Source ClinicalTrials.gov
Outcome
- Type
- SECONDARY
- Title
- Severe Maternal Morbidity
- Description
- Abstracted from delivery record: including postpartum hemorrhage, anemia requiring transfusion, sepsis, seizure, HELLP syndrome or preeclampsia with pulmonary edema
- Time frame
- Delivery
- Population
Source ClinicalTrials.gov
Trial
- Title
- Folic Acid and Zinc Supplementation Trial (FAZST)
- NCT number
- NCT01857310
- Phases
- NA
- Conditions
- Pregnancy, Live Birth, Spontaneous Abortion
- Interventions
- 5 mg folic acid and 30 mg elemental zinc, Placebo Comparator: Placebo
- Lead sponsor
- Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
- Results first posted
- 2020-11-19
- Results on ClinicalTrials.gov
- https://clinicaltrials.gov/study/NCT01857310?tab=results
Source ClinicalTrials.gov
Source
- Release
- trial-comparisons-2026-03-23-0.1.0
- Release manifest SHA-256
- f66225897fbf258b57ea10bdacfd0347d3cdfda93f7f5685234b7e06ea36fa57
- AACT copy
- 2026-03-23
- Tables read
- outcome_counts.parquet, outcome_measurements.parquet, outcomes.parquet, reported_event_totals.parquet, reported_events.parquet, result_groups.parquet, studies.parquet, ctgov_trial.parquet
Source ClinicalTrials.gov
Sources 2
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
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
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.
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