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Comparison · NCT02932475-1ce85a1c

Metformin vs Placebo: Number of Participants With Composite Adverse Neonatal Outcome

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. Metformin vs Placebo: Number of Participants With Composite Adverse Neonatal Outcome. Trial comparisons, record NCT02932475-1ce85a1c. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT02932475-1ce85a1c

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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 10.6970.6490.741wilson
Risk in group 20.7250.6780.767wilson
Risk difference, group 1 minus group 2-0.0282-0.0920.0358newcombe hybrid score
Risk ratio, group 1 over group 20.9610.8781.05log
Odds ratio, group 1 over group 20.8720.6381.19log
Number needed to treat, for one fewer participant with the outcome on Metformin than on Placebo35.4from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1MetforminMetformin 1000 mg twice a day269386OG000
Group 2PlaceboPlacebo, identical to Metformin. Delivered to match active drug277382OG001

Outcome

Type
PRIMARY
Title
Number of Participants With Composite Adverse Neonatal Outcome
Description
Participants with one or more of the following:~* capillary blood glucose level of \< 30 mg/dL or capillary blood glucose requiring medical treatment, or~* Birth trauma (umbilical cord artery pH \< 7.0 or shoulder dystocia with brachial plexus injury), or~* Hyperbilirubinemia requiring phototherapy, or~* Deliver \< 37 weeks' gestation, or~* Miscarry, are stillborn, experience a neonatal demise, or~* Large for gestational age infant (birth weight \> 90th percentile for gestational age), or~* Small for gestational age infant (birth weight \< 10th percentile for gestational age) or low birth weight (\< 2500 gm)
Time frame
An average of 48 hours for term infants and 30 days for preterm infants
Population
Modified intent to treat population of all participants who took at least one dose of study agent and had primary outcome data available.

Source ClinicalTrials.gov

Trial

Title
Medical Optimization of Management of Type 2 Diabetes Complicating Pregnancy (MOMPOD)
NCT number
NCT02932475
Phases
PHASE3
Conditions
Diabetes, Pregnancy
Interventions
Metformin, Placebo
Lead sponsor
University of North Carolina, Chapel Hill
Results first posted
2023-05-24

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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