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Comparison · NCT01355159-76f18d6c

Folic Acid 4 mg vs Placebo: Spontaneous Abortion

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: Spontaneous Abortion. Trial comparisons, record NCT01355159-76f18d6c. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT01355159-76f18d6c

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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 10.0230.01590.0333wilson
Risk in group 20.01780.01170.0271wilson
Risk difference, group 1 minus group 20.00524-0.006460.0172newcombe hybrid score
Risk ratio, group 1 over group 21.290.7362.28log
Odds ratio, group 1 over group 21.30.7322.32log
Number needed to treat, for one more participant with the outcome on Folic Acid 4 mg than on Placebo191from 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
271,172OG000
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.211,180OG001

Outcome

Type
SECONDARY
Title
Spontaneous Abortion
Description
Spontaneous abortion or miscarriage defined as death of a fetus \<500g or \<20 weeks of gestation
Time frame
Participants will be followed from randomization until 20+0 weeks of gestation
Population
Not all participants had secondary outcome data. Numbers above reflect those that had information available for this secondary outcome.

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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