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临床试验/NCT05772507
NCT05772507招募中不适用

Assessment of the Efficacy and Tolerance of URGO AWC_008 and URGO AWC_022 Dressings in Local Management of Acute and Chronic Wounds at Risk of Local Infection or With Clinical Signs of Local Infection

Laboratoires URGO1 个研究点 分布在 1 个国家目标入组 85 人开始时间: 2023年8月22日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
85
试验地点
1
主要终点
relative wound area reduction (RWAR)

研究概览

简要总结

Evaluation of the efficacy (wound epithelialization and time to closure) and tolerance (emergence and nature of adverse event) of the new URGO AWC_008 and URGO AWC_022 dressings in local management of acute and chronic wounds at risk of local infection or with clinical signs of local infection

详细描述

prospective multicenter, non comparative clinical investigation

This is a prospective multicenter, non comparative open-label, clinical investigation conducted in patients with acute and chronic wounds at risk of local infection or with clinical signs of local infection.

This study is carried out in France and Spain in around 30 investigator sites. A total of 85 patients meeting the eligibility criteria will be included. The patients will be followed for 4 weeks and a total of 5 clinical evaluations will be carried out by the investigating centers.

A planimetric survey of the studied wounds is carried out during the initial assessment of the wound (Day 0) and at each assessment provided for in the protocol (Week 1, Week 2, Week 3 and Week 4).

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

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

  • 未提供

排除标准

  • Patient with a wound for which treatment in a hyperbaric chamber is planned within 4 weeks following inclusion,
  • Patient with a serious general condition, that could lead to withdrawal from the trial before four weeks of treatment,
  • Patient who has experienced an acute ischaemic event (acute myocardial infarction or stroke) during the 3 months prior to inclusion in the investigation,
  • Patient with a systemic infection
  • Wound totally or partially covered on its surface with a black plaque of necrosis,
  • Cancerous wound

结局指标

主要结局

relative wound area reduction (RWAR)

时间窗: 4 week treatment period

changes in the area of wounds after 4 weeks of treatment.

次要结局

  • percentage of patients whose wound has healed(4 week treatment period)
  • Nature and incidence of Treatment Adverse Effects as assessed in percentage for each dressing(4 week treatment period)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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