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临床试验/EUCTR2019-003399-38-LV
EUCTR2019-003399-38-LV进行中(未招募)1 期

Effects of semaglutide on functional capacity in patients with type 2 diabetes and peripheral arterial disease

ovo Nordisk A/S0 个研究点目标入组 800 人开始时间: 2021年4月22日最近更新:
适应症
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
入组人数
800

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • - Male or female, age above or equal to 18 years at the time of signing informed consent.
  • For Japan and Taiwan: Male or female, age above or equal to 20 years at the time of signing informed consent, Appendix 8.
  • - Diagnosed with type 2 diabetes mellitus at least 180 days prior to the day of screening.
  • - Symptomatic PAD with intermittent claudication corresponding to Fontaine stage IIa (Rutherford classification grade I, category 1 and 2) meeting all of the following:
  • a. Stable symptoms of PAD with intermittent claudication in Fontaine stage IIa (able to walk without stopping more than 200 m/656 feet/2 blocks) for at least 90 days prior to the day of screening based on patient interview.
  • b. Screening flat treadmill test (3.2 km/h (2 mph)): Pain-free walking distance of equal to or above 200 meters/656 feet.
  • c. Screening constant load treadmill test with fixed inclination of 12% and a fixed speed of 3.2 km/h (2 mph): Walking distance equal to or below 600 meters/1968 feet.
  • d. Ankle-brachial-index (ABI) equal to or below 0.90 or toe-brachial index (TBI) equal to or below 0.70 (the leg with lowest index is chosen in case of bilateral disease).
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 320
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 480

排除标准

  • - Current or previous treatment with any GLP-1 receptor agonist (GLP-1-RA) within 90 days prior to the day of screening.
  • - Walking ability limited by conditions other than PAD (e.g. aortic aneurism, dysregulated arrhythmia or hypertension, angina pectoris, heart failure, chronic obstructive or restrictive pulmonary disease, Parkinson’s disease, severe peripheral neuropathy, amputations, wheel chair or walker dependency, osteoarthritis, morbid obesity, severe varicose veins, etc.).
  • - Planned orthopaedic surgery in the legs, or other major surgery known on the day of screening (surgery affecting walking ability).
  • - Vascular revascularisation procedure of any kind 180 days prior to the day of screening.
  • - Planned arterial revascularisation known on the day of screening.
  • - Myocardial infarction, stroke, hospitalisation for unstable angina pectoris or transient ischemic attack within 180 days prior to the day of screening.
  • - Heart failure presently classified as being in New York Heart Association (NYHA) class III-IV.

研究者

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