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临床试验/NCT00300339
NCT00300339已完成2 期

Double-Blind, Double-Dummy, Randomized, Parallel Group Trial of SL650472 (Three Dose Regimens Versus Placebo and Cilostazol), for 24-Week Improvement of Walking Distance in Patients With Stage II Peripheral Arterial Disease Who Benefit From Optimal Prevention Strategy Including Clopidogrel

Sanofi9 个研究点 分布在 9 个国家目标入组 599 人开始时间: 2006年2月1日最近更新:
适应症
相关药物

试验速览

阶段
2 期
状态
已完成
发起方
Sanofi
入组人数
599
试验地点
9
主要终点
Primary: percent change in initial claudication distance (ICD) measured at the 24-week test, compared with that at baseline

研究概览

简要总结

To investigate in patients suffering from intermittent claudication due to Fontaine stage II PAD whether a 24-week treatment by SL650472 OD on top of clopidogrel may result in an improvement of walking capacity, by comparing three doses of SL650472 to placebo, and to calibrate such effect versus cilostazol

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double (Participant, Investigator)

入排标准

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

入选标准

  • 1. Patient with stable symptoms of intermittent claudication of the lower extremities, secondary to chronic occlusive arterial disease from atherosclerosis origin (symptoms present for 6 months or longer and not significantly changed within the past 3 months);
  • 2. ICD of 30 to 200 m at screening constant workload treadmill test
  • 3. Doppler-measured pre-treadmill ABI of 0.90 or lower after 10 minutes of rest or, for patients with an ABI of greater than 1.3 (non-compressible arteries), a Toe-Brachial Index (TBI) of less than 0.7.

排除标准

  • 1. Age below 40 years and/or onset of symptoms of PAD before the age of 40 years;
  • 2. Non-atherosclerotic vascular disease (e.g. Buerger's disease, popliteal entrapment syndrome);
  • 3. Limb-threatening (grades III and IV) chronic limb ischemia, manifested by ischemic rest pain, ulceration, or gangrene.
  • 4. Patients with a history of malignant or proliferate breast disease.

结局指标

主要结局

Primary: percent change in initial claudication distance (ICD) measured at the 24-week test, compared with that at baseline

次要结局

  • Success, defined as an improvement of > 50% in ICD at the 24-week test compared with that at baseline
  • Percent change in absolute claudication distance (ACD) at the 24-week test, compared with that at baseline,
  • Functional status / quality of life (QoL) using WIQ and MOS SF-36 questionnaires,
  • Hemodynamic measurement post treadmill test (ABI/TB).

研究者

发起方
Sanofi
申办方类型
Industry

研究点 (9)

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