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Comparison · NCT01355159-6820d39e

Folic Acid 4 mg vs Placebo: Premature Rupture of Membranes

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

2 sourcestrial-comparisons-2026-03-23-0.1.0

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ConductScience Library. Folic Acid 4 mg vs Placebo: Premature Rupture of Membranes. Trial comparisons, record NCT01355159-6820d39e. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT01355159-6820d39e

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Measures6

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

MeasureValue95% interval, lower95% interval, upperMethodNote
Risk in group 10.1840.1630.207wilson
Risk in group 20.190.1680.213wilson
Risk difference, group 1 minus group 2-0.00591-0.03740.0256newcombe hybrid score
Risk ratio, group 1 over group 20.9690.8181.15log
Odds ratio, group 1 over group 20.9620.7821.18log
Number needed to treat, for one fewer participant with the outcome on Folic Acid 4 mg than on Placebo169from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Folic Acid 4 mg
Folic Acid 1.0 mg x 4 tablets will be taken daily by oral administration. The majority of women in the study will routinely take 1.0 mg folic acid in a prenatal vitamin supplement, as recommended by their primary obstetrical provider; the study requirements do not require that participants change their practice. Therefore the actual total daily dose may be up to 5.1 mg of folic acid~Folic Acid 4 mg: Folic Acid 1.0 mg or placebo x 4 tablets will be taken daily by oral administration. The majority of women in the study will routinely take 1.0 mg folic acid in a prenatal vitamin supplement, as recommended by their primary obstetrical provider; the study requirements do not require that participants change their practice. Therefore the actual total daily dose may be up to 5.1 mg of folic acid
2151,169OG000
Group 2PlaceboWomen will be randomised in a 1:1 ratio to folic acid 4.0 mg or placebo~Placebo: Placebo x 4 tablets will be taken daily by oral administration.2241,180OG001

Outcome

Type
SECONDARY
Title
Premature Rupture of Membranes
Description
Rupture of the membranes (rupture of the amniotic sac) before the onset of labor.
Time frame
Participants will be followed from randomization (8-16 weeks' completed gestation) until the onset of labor
Population

Source ClinicalTrials.gov

Trial

Title
High Dose Folic Acid Supplementation Throughout Pregnancy for Preeclampsia Prevention
NCT number
NCT01355159
Phases
PHASE3
Conditions
Pregnancy Complications, Preeclampsia
Interventions
Folic Acid 4 mg, Placebo
Lead sponsor
Ottawa Hospital Research Institute
Results first posted
2020-07-07

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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