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Dallas, Texas 75235


This is a randomized prospective trial which addresses the question of whether use of an oral hypoglycemic agent as an adjunct to diet therapy in women with mild gestational diabetes will result in achieving euglycemia in a shorter period of time and, in turn, result in less frequent maternal and neonatal morbidities. This study is designed to test the hypothesis that in women with mild GDM, use of Glyburide in addition to diet and nutritional counseling lowers mean infant birth weight by 200 grams as compared with diet and nutritional counseling alone.


Inclusion Criteria: - A glucose value of ≥140 mg/dl on a 50-gram oral glucose loading test by plasma at gestational age between 24 weeks 0 days and 27 weeks 6 days based on clinical information - An Abnormal 3-hour oral glucose tolerance test with a fasting glucose of ≤105 mg/dl - Gestational age of less than or equal to 28 weeks and 0 days at the time of consent/randomization - Singleton gestation Exclusion Criteria: - Established pregestational diabetes - Abnormal gestational diabetes testing (≥140) prior to 24 weeks 0 days of gestation. Women who have a negative glucose loading test (<140mg/dl) before 24 weeks may still be considered for this study if they present again for glucose tolerance testing between 24 and 27 weeks. - Multiple gestations - Known major fetal anomaly or fetal demise - Any renal disease with serum creatinine of >1.0 - Known liver disease such as hepatitis - Maternal or fetal conditions likely to require imminent or very preterm delivery such as preeclampsia, preterm premature rupture of the membranes, preterm labor, and intrauterine fetal growth restriction - Known hypersensitivity or allergic reaction to Glyburide



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Dallas, Texas 75235
United States

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Site Status: N/A

Data Source: ClinicalTrials.gov

Date Processed: October 09, 2019

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