跳至主要内容
临床试验/NCT02176681
NCT02176681
已完成
4 期

A Prospective, Multicenter, Randomized, Open-label Study of 12 Week Duration to Evaluate the Effect of VILDagliptin Added to Insulin on Glycaemic Control in haemoDIALyzed Patients With Type 2 Diabetes: Probe Analysis of CGM

University Hospital, Strasbourg, France24 个研究点 分布在 1 个国家目标入组 70 人2014年6月1日

概览

阶段
4 期
干预措施
Insulin
疾病 / 适应症
Haemodialyzed, Type 2 Diabetes
发起方
University Hospital, Strasbourg, France
入组人数
70
试验地点
24
主要终点
Mean glucose value of CGM [M] to be averaged from day 2 and day 3 of CGM
状态
已完成
最后更新
上个月

概览

简要总结

Diabetes is a major concern for dialysis units, as it is now the most common cause of end-stage renal disease in France. In 2010 at initiation of dialysis treatment, more than one patient out of two had at least one cardiovascular disease and 40 % diabetes (94 % Type 2 diabetes) and especially in East part of France.

Diabetic patients on dialysis have a high burden of morbidity and mortality, particularly from cardiovascular disease. Tight glycaemic and blood pressure control in diabetic patients has an important impact in reducing risk of progression nephropathy. Data are scarce on how diabetes should best be treated in dialysis patients. The evidence for improving glycaemic control in patients on dialysis having an impact on mortality or morbidity is sparse. Indeed, many factors make improving glycaemic control in patients on dialysis very challenging, including therapeutic difficulties with hypoglycaemic agents, monitoring difficulties, dialysis strategies that exacerbate hyperglycaemia or hypoglycaemia.

Standard oral drugs therapy for hyperglycaemia (eg, metformin, sulfonylureas, ) are contraindicated in patients on dialysis. Thus insulin has been the mainstay of treatment. Newer therapies for hyperglycaemia, such as gliptins and glucagon-like peptide-1 analogues have become available, but until recently, renal failure has precluded their use. Newer gliptins, however, are now licensed for use in 'severe renal failure', although they have yet to be trialed in dialysis patients.

The investigators study, using continuous glucose monitoring as a new tool for monitoring of therapy should provide information on vildagliptin in add on therapy to insulin in this population.

注册库
clinicaltrials.gov
开始日期
2014年6月1日
结束日期
2017年10月1日
最后更新
上个月
研究类型
Interventional
研究设计
Parallel
性别
All

研究者

发起方
University Hospital, Strasbourg, France
责任方
Sponsor

入排标准

入选标准

  • Patients treated by haemodialysis for more than 3 months with 1g/L glucose in dialysate fluid
  • Patients treated by stable doses of insulin (any regimen) for Type 2 diabetes without any oral antidiabetic agent
  • Age \> 18 years
  • TGO, TPO and lipase \< 3x ULN
  • effective means of contraception
  • Non-inclusion Criteria:
  • Blood transfusion in the 2 previous months
  • Life expectancy less than 1 year
  • Chronic inflammatory disease
  • Steroid treatment \> 5mg/day

排除标准

  • 未提供

研究组 & 干预措施

Insulin alone

Use the usual frequency and dose

干预措施: Insulin

Insulin and Vildagliptin

vildagliptin 50 mg/day during 3 months

结局指标

主要结局

Mean glucose value of CGM [M] to be averaged from day 2 and day 3 of CGM

时间窗: up to day 3

次要结局

  • CGM parameters at baseline and month 3(Other CGM parameters at baseline and month 3)
  • Number of hypoglycaemic events(Hypoglycaemic events at baseline, month 3)
  • Mean HbA1C and Glycated albumin(HbA1C and Glycated albuminat baseline and month 3)

研究点 (24)

Loading locations...

相似试验