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临床试验/ISRCTN00928792
ISRCTN00928792已完成未知

Metformin in Women with Type 2 Diabetes in Pregnancy ? a randomized controlled trial

The Centre for Mother, Infant, and Child Research (CMICR) (Canada)0 个研究点目标入组 502 人开始时间: 2011年7月26日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
入组人数
502

研究概览

简要总结

2020 results in https://pubmed.ncbi.nlm.nih.gov/32946820/ (added 29/01/2021)

研究设计

研究类型
Interventional

入排标准

性别
Female

入选标准

  • 1. Women between the ages of 18-45
  • 2. Women diagnosed with type 2 diabetes prior to pregnancy or women with undiagnosed type 2 diabetes diagnosed prior to 20 weeks gestation [defined as women presenting with gestational diabetes before 20 weeks gestation with an elevated glycosylated hemoglobin (HbA1c) which is 8% or more above the upper normal range (i.e. HbA1c of 6.5% if upper normal is 6.0%, or HbA1c 7% if upper normal is 6.5%) or fasting glucose >= 7.0 mmol/L]
  • 3. Pregnancy gestation between 12 weeks 0 days - 22 weeks 6 days
  • 4. Live singleton fetus

排除标准

  • 1. Women who are not on insulin
  • 2. Women who are on oral hypoglycemic agents should be switched to insulin prior to randomization
  • 3. Diabetes diagnosed after 20 weeks gestation
  • 4. Type 1 diabetes
  • 5. Known intolerance to metformin
  • 6. Contraindications to metformin use which include:
  • 6.1 Renal insufficiency (defined as serum creatinine of greater than 130 umol/L or creatinine clearance < 60 ml/min
  • 6.2 Moderate to severe liver dysfunction (defined as liver enzymes aspartate aminotransferase (AST) and alanine aminotransferase (ALT)) greater than three times the upper limit of normal)
  • 6.3 Shock or sepsis
  • 6.4 Previous hypersensitivity to metformin
  • 7. Women with significant gastrointestinal problems such as severe vomiting requiring intravenous fluids or hospitalization, or active Crohn's or colitis
  • 8. Previous participation in the trial
  • 9. Patients who have a fetus with a known potentially lethal anomaly will be excluded. Information regarding congenital anomalies diagnosed after randomization will be recorded.
  • 10. Known higher order pregnancies (twins, triplets, etc). These women will be excluded as they have a higher rate of adverse outcomes and we want to avoid any inequalities if they are unequally distributed between the groups
  • 11. Presence of acute or chronic metabolic acidosis, including diabetic ketoacidosis
  • 12. History of diabetic ketoacidosis or history of lactic acidosis
  • 13. Presence of excessive alcohol intake, acute or chronic
  • 14. Presence of congestive heart failure or history of congestive heart failure

研究者

发起方
The Centre for Mother, Infant, and Child Research (CMICR) (Canada)

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