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Comparison · NCT00744965-457ec0e8

Glyburide vs Placebo: Macrosomia

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. Glyburide vs Placebo: Macrosomia. Trial comparisons, record NCT00744965-457ec0e8. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00744965-457ec0e8

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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 10.06880.04060.114wilson
Risk in group 20.09680.06210.148wilson
Risk difference, group 1 minus group 2-0.028-0.08620.0291newcombe hybrid score
Risk ratio, group 1 over group 20.7110.3591.41log
Odds ratio, group 1 over group 20.6890.3281.45log
Number needed to treat, for one fewer participant with the outcome on Glyburide than on Placebo35.7from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Glyburide
Women with mild gestational diabetes will be started ADA diet and a low dose of Glyburide and their medication dosage will be titrated as necessary during the pregnancy to achieve glucose control.~Glyburide: Starting dosage is 2.5 mg once daily. This dose will be titrated as necessary during the pregnancy to achieve glycemic control.
13189OG001
Group 2PlaceboWomen with mild gestational diabetes will be started ADA diet and placebo.~Placebo: Sham dose adjustments of the placebo will be made.18186OG000

Outcome

Type
SECONDARY
Title
Macrosomia
Description
birth weight 4,000 g or greater
Time frame
After delivery
Population

Source ClinicalTrials.gov

Trial

Title
Treatment of Mild Gestational Diabetes With Glyburide Versus Placebo
NCT number
NCT00744965
Phases
PHASE4
Conditions
Mild Gestational Diabetes
Interventions
Glyburide, Placebo
Lead sponsor
University of Texas Southwestern Medical Center
Results first posted
2020-03-12

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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