跳至主要内容
临床试验/ISRCTN70770260
ISRCTN70770260已完成2 期

Safety, tolerability and effectiveness of Glucophage® SR in patients with type 2 diabetes and chronic Kidney disease

West Wales Hospital (UK)0 个研究点目标入组 50 人开始时间: 2012年3月7日最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
50

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

性别
All

入选标准

  • 1. Age > 18 years
  • 2. Male or female
  • 3. Patients with Type 2 diabetes
  • 4. Suboptimal glycaemic control {HbA1c = 7.5% (IFCC equivalent = 58mmol/mol)} at the screening visit
  • 5. Chronic kidney disease with Estimated Glomerular Filtration Rate (eGFR) = 30mL/minute/1.73m2 to = 45mL/minute/1.73m2 at the screening visit
  • 6. Stable renal function (eGFR) in the last 3 months
  • 7. Willing and able to comply with the study protocol

排除标准

  • 1. Previous myocardial infarction (MI) (in last 6 months)
  • 2. Previous history of Congestive Cardiac Failure New York Heart Association (NYHA) class III or IV
  • 3. Previous history of Chronic obstructive pulmonary disease (COPD)
  • 4. Chronic kidney disease with eGFR < 30mL/minute/1.73m2
  • 5. Abnormal alanine aminotransferase (ALT) (> 3fold at baseline)
  • 6. Hypoglycaemia symptoms unawareness
  • 7. History of hypoglycemic episodes requiring 3rd party assistance for reversal in last 12 months
  • 8. Uncontrolled Hypertension (BP > 180/100mmHg)
  • 9. Pregnant or likelihood of pregnancy during the study
  • 10. Females who are breastfeeding
  • 11. Proliferative Diabetic retinopathy and/or laser treatment in last 6 months
  • 12. History of Diabetic ketoacidosis, lactic acidosis and gasteroparesis
  • 13. Current treatment with metformin/Glucophage® SR
  • 14. Treatment with metformin/Glucophage® SR in last 3 months prior to screening visit
  • 15. History of irritable bowel syndrome
  • 16. Previous intolerance to metformin or Glucophage® SR
  • 17. Patients currently on dipeptidyl peptidase IV (DPPIV) inhibitors and Glucagon-Like Peptide (GLP) analogues
  • 18. History of significant (more than one stone) weight loss in last 6 months
  • 19. History of allergic or hypersensitivity reaction to metformin, Glucophage® SR or any insulin
  • 20. Patients unable to tolerate minimum 1000mg daily divided dose of Glucophage® SR
  • 21. Any other condition excluded in Summary of Product Characteristics (SPC)

研究者

发起方
West Wales Hospital (UK)

相似试验