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临床试验/NCT04710563
NCT04710563进行中(未招募)不适用

SCOPE-CLI: Shifting Care and Outcomes for Patients With Endangered Limbs - Critical Limb Ischemia

Yale University1 个研究点 分布在 1 个国家目标入组 458 人开始时间: 2021年8月11日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
458
试验地点
1
主要终点
Peripheral Artery Questionnaire (PAQ)

研究概览

简要总结

A research project capturing experiences of patients with critical limb threatening ischemia, with the ultimate goal of setting new standards for diagnosing, describing detailed patient-centered outcomes, and evaluating the variability in therapeutic approaches and their association with outcomes.

详细描述

An estimated 8 million individuals in America are affected by peripheral arterial disease (PAD). One of its extreme expressions is Critical Limb Ischemia (CLI). It is one of the most severe vascular conditions associated with devastating outcomes, including poorly healing wounds, extreme pain, and a high amputation risk. It is also one of the deadliest conditions, with 6-month and 5-year mortality rates estimated to be 20 and >50%, respectively. To date, however, there is a paucity of prospective clinical evidence about the variability in patients' presentations, their management or their outcomes. Accordingly, little progress has been made in adequately staging the disease and to risk-stratify treatment approaches to patients' individual characteristics. What is desperately needed to advance the care and management of patients with CLI is a focused research effort to set new standards for diagnosing, describing detailed patient-centered outcomes, and evaluating the variability in therapeutic approaches and their association with outcomes. The specific aims of SCOPE-CLI are to generate new evidence on the clinical characteristics, treatment patterns and outcomes of patients with critical limb ischemia (CLI); to describe treatment patterns and variability across practices to identify gaps in delivering quality care; and to perform a series of analyses to examine the associations of patient and treatment characteristics with outcomes. The central objective of SCOPE-CLI is to systematically quantify patients' CLI-specific health status and clinical outcomes and to perform subgroup analyses as a function of different PAD treatments and patient characteristics.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

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

  • All race/ethnicity categories, English speaking, men and women
  • Patient presents with current (within 30 days) Rutherford Class 4, 5, or 6
  • Age ≥18 years
  • Supported by any of the following diagnostic evidence:
  • Rutherford Classification 4 or ischemic rest pain and/or resting ankle pressure <50mmHg, flat or barely pulsatile ankle or metatarsal PVR or toe pressure <40mmHg
  • Rutherford Classification 5 or minor tissue loss; non-healing ulcer, focal gangrene with diffuse pedal ischemia resting ankle pressure <50mmHg ankle or metatarsal PVR flat or barely pulsatile or toe pressure <40mmHg
  • Rutherford Classification 6 or major tissue loss: extending above transmetatarsal level, functional foot no longer salvageable, resting ankle pressure <50mmHg ankle or metatarsal PVR flat or barely pulsatile or toe pressure <40mmHg
  • CLI related ICD 10 code (reason for admission or indication for procedure)
  • SPP < 50 mmHg
  • TCPO2 < 50 mmHg
  • Angiographic evidence no straight line to foot or greater than 70% stenosis in all 3 lower extremity arteries (AT, PT, peroneal)
  • ABI* ≤ 0.90
  • non-compressible ABI ≥ 1.40 AND TBI ≤ 0.70
  • TBI* ≤ 0.70

排除标准

  • Acute limb ischemia
  • Unable to provide written informed consent
  • Currently a prisoner (identified at time of enrollment)

结局指标

主要结局

Peripheral Artery Questionnaire (PAQ)

时间窗: After enrollment and follow-up at month 12

PAD-specific, multi-dimensional health status instrument with a CLI specific module. Higher scores indicate better functioning.

次要结局

  • Amputation Free Survival (AFS)(5 years after enrollment)
  • Major adverse limb events (MALE)(5 years after enrollment)
  • Mortality - Death(5 years after enrollment)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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