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临床试验/NCT03640026
NCT03640026终止4 期

Glucose Disorders Induced by Tacrolimus on Pre Transplantation Endstage Renal Disease Patients

Centre Hospitalier Departemental Vendee4 个研究点 分布在 1 个国家目标入组 61 人开始时间: 2019年3月8日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
终止
入组人数
61
试验地点
4
主要终点
Proportion of haemodialysis patients modifying their glycemic profile receiving Tacrolimus

研究概览

简要总结

Diabetes after kidney transplantation is a frequent complication, the incidence of which varies from 7 to 45% depending on the studies and on the diagnostic criteria used. Post-transplant diabetes is an early complication, most often occurring in the first month after transplantation.

In addition to the additional health costs generated by the appearance of post-transplant diabetes, the risk of graft loss is increased by 60% and the overall mortality risk by 90%. Similarly, the development of glucose intolerance after transplantation is associated with higher mortality.

Tacrolimus treatment is therefore currently one of the most important risk factors for diabetes at the time of transplantation.

Indeed, several in vitro and in vivo animal studies have shown that tacrolimus alters pancreatic endocrine function.

In the final stage, this cellular toxicity leads to diabetes, most often diagnosed on the rise in capillary or venous blood sugar levels after transplantation. This diabetes often requires hypoglycemic treatment with insulin or oral anti-diabetic drugs. for a variable period. The pro-diabetogenic effect of tacrolimus is sometimes irreversible, justifying preventive treatment.

No clinical studies have looked at "sub-clinical" changes in insulin secretion or insulin resistance under tacrolimus prior to the onset of diabetes. The static indices HOMA-β% and HOMA-IR (Homeostasis Model Accessment of insulin resistance) make it possible to estimate insulin secretion and insulin resistance in fasting patients respectively, while the oral glucose disposition index (IDO) makes it possible to study insulin secretion and action dynamically (after a 75 g glucose load), and are calculated as follows:

HOMA IR= Fasting blood glucose (mmol/L) x Fasting insulin (mU/L)/ 22.5 HOMAβ% = 20 x fasting insulinemia (mU/L) / fasting plasma glucose (mmol/L) - 3.5 IDO = (delta insulinemia T30-T0/ delta blood glucose T30-T0)/insulinemia T0

These indices have already been studied in dialysis patients (diabetic and non-diabetic) and may allow a more detailed study of pancreatic response and insulin resistance under tacrolimus in patients prior to renal transplantation. Determining the "pancreatic response" to tacrolimus in patients prior to transplantation would prevent diabetes by adapting immunosuppressive treatment and post-transplant screening modalities in the event of pre-transplant subclinical abnormalities identified in our study. The development of tacrolimus-induced diabetes in pre-transplantation in our study will be a contraindication to tacrolimus at the time of transplantation and ciclosporin therapy will be preferred.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Diagnostic
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age ≥ 18 years
  • Patient eligible for kidney transplantation at the Nantes University Hospital
  • Hemodialysis patient in one of the participating centres
  • Patient who is able to understand the proposed protocol and has given free and informed consent
  • Patient with affiliation to the French social security system.

排除标准

  • Personal history of diabetes treated or untreated
  • Temporary contraindication for carcinological reasons
  • Immunosuppressive treatment in the 6 months prior to inclusion
  • Macrolide Allergies
  • Hypersensitivity to the excipients used in the composition of tacrolimus
  • Intolerance to the HGPO test
  • Progressive infectious outbreak
  • Hepatic insufficiency
  • Intercurrent infectious pathology
  • Patient under guardianship, curatorship, legal protection measure, or deprived of liberty
  • Pregnant women, breastfeeding, or non-menopausal woman who refuses contraception

研究组 & 干预措施

Tacrolimus treatment

Experimental

干预措施: Tacrolimus (Drug)

结局指标

主要结局

Proportion of haemodialysis patients modifying their glycemic profile receiving Tacrolimus

时间窗: During 14 days

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (4)

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