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临床试验/ISRCTN01772998
ISRCTN01772998已完成未知

Allopurinol as a possible oxygen sparing agent during exercise in peripheral arterial disease: a double-blind, placebo-controlled, parallel group study

niversity of Dundee (UK)0 个研究点目标入组 50 人开始时间: 2010年10月25日最近更新:
适应症

试验速览

阶段
未知
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. Men and women age 35-85 years suffering from PAD. PAD will be defined as:
  • 1.1. Claudication defined as leg pain on walking and disappearing within 10 minutes on standing and of presumed atherosclerotic origin
  • 1.2. An ankle brachial pressure index (ABPI) of <0.90 on the worst leg at rest
  • 2. Stable disease demonstrated by having a reproducible pain free walking distance on 2 consecutive treadmill tests, i.e. less than 25% variance. The reason for termination of the test must be claudication pain only. All treadmill tests will be done at a speed of 3.2 km/h (= 2 mph), as is standard practice in PAD trials. The incline will begin at 0% and increase in grade of 2% every 2 minutes. This is the standard Skinner-Gardner protocol (Angiology 1992, 43(8): 661-671).

排除标准

  • 1. Rest pain
  • 2. Childbearing potential
  • 3. Heart failure
  • 4. Any other exercise limiting cardiac disease
  • 5. BP >180/100 mHg
  • 6. eGFR <60 ml/min
  • 7. Liver disease
  • 8. Malignancy
  • 9. Already on allopurinol or had an adverse reaction to it.
  • 10. Participants who have had a recent marked change in symptoms or recent (in the last six months) intervention for PAD
  • 11. Participants receiving treatment which is contraindicated with the study treatment
  • 11.1. 6-mercaptopurine
  • 11.2. Azathioprine
  • 11.3. Warfarin
  • 11.4. Theophylline

研究者

发起方
niversity of Dundee (UK)

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