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临床试验/NCT01687582
NCT01687582已完成不适用

Clinical and Histopathological Effect of GLP-1 Analogs on Psoriasis in Type 2 Diabetic Patients

Cliniques universitaires Saint-Luc- Université Catholique de Louvain1 个研究点 分布在 1 个国家目标入组 10 人开始时间: 2012年1月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
10
试验地点
1
主要终点
Improvement of PASI score

研究概览

简要总结

The aim of the study is to evaluate after 4 to 6 months the effects of a GLP-1 analog treatment on psoriatic skin lesions in patients with type 2 diabetes.

详细描述

The objective of this study is to analyse short and medium-term efficacy on clinical, immunological and histopathological parameters of a GLP-1 receptor agonist on moderate to severe psoriasis plaques in a group of patients with type 2 diabetes.

研究设计

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

入排标准

年龄范围
20 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Type 2 diabetic patients treated with oral anti-hyperglycaemic agents and/or insulin and presenting stable psoriasis plaques for at least one year, which failed to respond to previous systemic and/or topical treatments.

排除标准

  • Type 1 diabetes
  • Secondary diabetes
  • Liver, renal or pancreatic disease
  • Previous treatment with GLP-1 agonist or DPP-4 inhibitors agents

研究组 & 干预措施

GLP-1 analog

Experimental

Liraglutide, 0.6 to 1.8 mg per day or Exenatide, 5 to 10 µg twice a day.

干预措施: GLP-1 analog (Drug)

结局指标

主要结局

Improvement of PASI score

时间窗: 4 to 6 months

次要结局

  • Evolution of BMI(4 to 6 months)
  • Evolution of immunological data(4 to 6 months)
  • Evolution of BMI (body mass index)(4 to 6 months)
  • Evolution of histopathological data(4 to 6 months)
  • Evolution of glycaemic control(4 to 6 months)
  • Evolution of routine laboratory measures(4 to 6 months)

研究者

发起方
Cliniques universitaires Saint-Luc- Université Catholique de Louvain
申办方类型
Other
责任方
Sponsor

研究点 (1)

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