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临床试验/NCT04939038
NCT04939038终止不适用

Timing of Revascularization in Patients With Diabetic Foot Ulcer and Non-critical Peripheral Artery Disease: a Randomized, Controlled Trial

Insel Gruppe AG, University Hospital Bern4 个研究点 分布在 1 个国家目标入组 10 人开始时间: 2022年1月25日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
终止
入组人数
10
试验地点
4
主要终点
Number of patients with Minor amputation

研究概览

简要总结

This study investigates whether, compared to standard treatment, immediate restoration of blood flow (revascularization) can reduce complications and improve diabetic foot ulcer healing.

详细描述

Background: In approximately 80% of diabetes-related lower extremity amputations, patients suffer from a foot ulcer, often caused by lower extremity arterial disease. Due to lower extremity arterial disease (LEAD), diabetic patients with foot ulcers often require lower limb amputation. Achieving arterial supply (revascularization) to the ulcer is the most important factor in healing the diabetic foot ulcer and reduces the risk of amputation. The current standard of care recommends revascularization after six weeks in patients with low-grade arterial disease of the lower extremities and nonhealing foot ulcer. The aim of this study is to demonstrate that in patients with low grade arterial disease of the lower extremities and diabetic foot ulcers, immediate revascularization results in fewer cardiovascular problems and amputations, as well as improved ulcer healing, compared to the current standard of care.

Study procedure: After inclusion in the study, participants will be randomized into the control arm or the active arm. In the control arm standard wound care will be performed. In the active arm, revascularization will be performed on top of standard wound care within 7 days after randomization. Post-revascularization analysis on ankle- and toe pressure, laboratory analysis, and wound care team assessment and therapy will be performed 24 h post operation.

Follow up will be on 45, 90, 180 and 365 day for patients of both arms, where ankle- and toe pressure, laboratory analysis, and wound care team assessment and therapy will be performed.

Number of Participants: 240 participants in total, 120 per treatment arm

Study duration: 4 years

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
Single (Outcomes Assessor)

入排标准

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

入选标准

  • •Informed consent as documented by signature
  • •Patients that are at least 18 years old
  • •Patients that have at least one DFU(s) of ≥ 0.2 cm2 and ≤ 10 cm2 as assessed by the ruler method multiplying the greatest length and width of the ulcer after debridement to determine the surface area. The largest eligible ulcer (≤ 10 cm2) will be defined as index ulcer and the corresponding extremity as index limb (in case of multiple equally sized ulcers the following rules will apply: If on different feet, the dominant side and if on the same foot, the more peripheral one will be the index ulcer)
  • •Patients that have non-critical LEAD of the index leg, defined by a single non-invasive examination at screening:
  • •Ankle brachial index (ABI) ≥ 0.5 and ≤ 0.9 AND absolute ankle pressure ≥ 50 mmHg OR
  • •ABI > 0.9 OR incompressible ankle pressures AND toe brachial index (TBI) ≤ 0.7 AND absolute toe pressure ≥ 30 mmHg
  • •Patients on medical treatment for glycemic control with diagnosis of diabetes mellitus that was assessed by criteria as recommended by the guideline 2019 "ESC Guidelines on diabetes, pre-diabetes, and cardiovascular diseases developed in collaboration with the EASD". Or patient without medical treatment but diagnosed with diabetes mellitus via HbA1c.
  • •Patients with life expectancy > 12 months and without any disabilities due to end-stage cancer, heart failure, severe chronic obstructive pulmonary disease (COPD), or dementia

排除标准

  • •Critical limb ischemia of the index leg defined as ABI ≤ 0.4 (or absolute ankle pressure < 50 mmHg)
  • •No option to assess for toe pressure due to any reason at baseline if ABI > 0.9 or incompressible ankle pressures and patient inclusion is based on the toe pressure criteria.
  • •Need for major amputation
  • •Severe infection at the index foot according to IDSA classification
  • •Patient refuses minor amputation despite strong recommendation due to severe infection, necrosis or osteomyelitis at screening assessment
  • •Any revascularization procedure at the index leg within 3 months before randomization
  • •Positive urine or blood pregnancy test result, breast feeding or intention to become pregnant
  • •Non-compliance for any reason to procedures or study assessments (e.g. due to cognitive impairment or geographic distance)
  • •Participation in another drug study within the 30 days preceding or during the present study
  • •Untreated known antiphospholipid antibody syndrome and polycythaemia vera
  • •Known significant bleeding risk, or known coagulation disorder (INR > 3.0 and platelet count < 30,000/mm3) without any option to correct within 7 calendar days after initial wound assessment

研究组 & 干预措施

Control Arm

Active Comparator

Standard wound care for diabetic wound ulcer

干预措施: Standard wound care (Procedure)

Immediate revascularization

Experimental

Patient will have revascularization 0 - 7 days after initial wound assessment and then receive standard wound care for diabetic wound ulcer

干预措施: Revascularization (Procedure)

Immediate revascularization

Experimental

Patient will have revascularization 0 - 7 days after initial wound assessment and then receive standard wound care for diabetic wound ulcer

干预措施: Standard wound care (Procedure)

结局指标

主要结局

Number of patients with Minor amputation

时间窗: up to 12 months after randomization

Number of patients with missed diabetic foot ulcer healing

时间窗: 90 days after randomization

i.e. Incomplete epithelization of the index ulcer at 90 days

Number of patients with non-fatal myocardial infarction or all-cause stroke

时间窗: up to 12 months after randomization

Number of patients with cardiovascular death

时间窗: up to 12 months

Number of patients with major amputation

时间窗: up to 12 months after randomization

Number of patients with delayed diabetic foot ulcer healing

时间窗: 45 days after randomization

Reduction of wound size of less than 50% at 45 days

次要结局

  • Number of patients with all clinically-driven revascularizations at the index limb(up to 12 months after randomization)
  • Number of in-hospital days and costs(up to 12 months after randomization)
  • Number of patients with new ulcer of the index foot(up to 12 months after randomization)
  • Each component of the primary outcome individually(up to 12 months after randomization)
  • Number of patients with major amputation-free survival(up to 12 months after randomization)
  • Number of patients with all-cause death(up to 12 months after randomization)
  • Change in quality of life (QoL) assessed by the Cardiff Wound Impact Schedule questionnaire(from baseline to 90 days and 12 months after randomization)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (4)

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