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临床试验/NCT06667752
NCT06667752招募中不适用

A Randomized, Double Blind, Active Controlled, Parallel Group Clinical Trial to Assess the Safety and Efficacy of Nanordica Antibacterial Wound Dressing in Patients With DFUs

Nanordica Medical OU12 个研究点 分布在 2 个国家目标入组 170 人开始时间: 2024年10月17日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
170
试验地点
12
主要终点
CWC at 12 weeks

研究概览

简要总结

This clinical trial evaluates the safety and efficacy of the Nanordica Advanced Antibacterial Wound Dressing (AAWD) in patients suffering from diabetic foot ulcers.

At least 170 participants will be randomly allocated to be treated either with AAWD or Aquacel Ag+ Extra wound dressing for a 4-week active phase (intervention) followed by an 8-week standard of care period.

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, 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

入选标准

  • Voluntary, written informed consent obtained prior to any study related activities.
  • Males and females aged ≥18 years.
  • DFU(s) present for more than 4 weeks with a maximum diameter of 4 cm.
  • IWGDF/IDSA Wound infection grades 1 (absent) or
  • Patients willing and able to comply with scheduled visits, laboratory sampling and study procedures.
  • Ankle-brachial index (ABI) 0.9-1.4 or ABI between 0.6-0.9 with ankle pressure ≥ 70 mmHg.

排除标准

  • Ssystemic or topical antibiotic therapy within 7 days before the enrolment.
  • Any wound with known associated osteomyelitis or positive probe-to-bone test.
  • Previous randomization in this clinical trial.
  • Surgical procedures in the same leg as the index ulcer(s) (e.g., radical debridement, ulcerectomy, skin grafting, exostectomy, amputation) within the past four weeks, or planned to during the study.
  • Use of other advanced therapies directly involving the index ulcer(s) (e.g. skin substitutes, matrices, cellbased therapies or products) within the past four weeks.
  • Patients suffering cardiac disorders grade NYHA IV.
  • Patients suffering hepatic disorders grade Child-Pugh C.
  • Stage 4 cancer.
  • Women of childbearing potential who are pregnant, breast-feeding or not using adequate contraceptive methods.

结局指标

主要结局

CWC at 12 weeks

时间窗: 12 weeks

complete wound closure (CWC) at 12 weeks

次要结局

  • CWC at 4 weeks(4 weeks)
  • Time to heal(Up to 12 weeks)
  • Adverse events(12 weeks)

研究者

发起方
Nanordica Medical OU
申办方类型
Industry
责任方
Sponsor

研究点 (12)

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