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临床试验/NCT07223892
NCT07223892尚未招募3 期

A Prospective Controlled Trial Evaluating the Efficacy of Carbonlife Amniotic Tissue Product in the Treatment of Chronic Wounds: A Stratified Analysis by Wound Etiology and Care Setting

Bardia Anvar0 个研究点目标入组 600 人开始时间: 2026年1月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
尚未招募
发起方
入组人数
600
主要终点
Wound Closure

研究概览

简要总结

Chronic wounds constitute a significant global health burden, affecting millions of individuals and contributing to increased morbidity, diminished quality of life, and rising healthcare costs. These wounds are characterized by delayed healing and are often associated with complex etiologies and prolonged treatment courses. This study aims to evaluate the clinical efficacy and cost-effectiveness of Carbonlife amniotic tissue products (ATPs) compared to standard wound care in the management of chronic wounds. A prospective, controlled clinical trial will be conducted across diverse care settings and patient populations with varying wound etiologies. Participants will be stratified by wound type and treatment environment to enable subgroup analyses. The primary endpoint will assess wound healing outcomes, while secondary endpoints will include quality-of-life measures and healthcare resource utilization. The study is designed to generate high-quality evidence regarding the therapeutic value of ATPs in chronic wound management. Stratified analyses will provide insights into the differential effectiveness of ATPs across clinical contexts. Findings are anticipated to have implications for clinical practice guidelines and healthcare policy, with the goal of improving patient outcomes and optimizing resource allocation in wound care.

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

  • •Facilities and centers with the capacity to follow strict treatment and care guidelines for patients.
  • •Adults aged 18 years or older.
  • •Presence of a chronic wound (defined as a wound that has not shown significant improvement in 4 weeks) of any of the following etiologies: Diabetic foot ulcers, Venous leg ulcers, Arterial ulcers, Pressure ulcers, Burns, Trauma, Surgical
  • •Wound size greater than 1 cm²
  • •Ability to provide informed consent

排除标准

  • •Presence of active osteomyelitis
  • •Untreated malignancy in the wound area
  • •Known allergy to components of ATPs
  • •Pregnant or breastfeeding women
  • •Patients receiving immunosuppressive therapy
  • •Patients with a life expectancy of less than 12 weeks

研究组 & 干预措施

ATP Treatment Group

Experimental

Application of Carbonlife ATP per manufacturer's instructions along with standard wound care.

干预措施: Amniotic Tissue Allograft (Biological)

结局指标

主要结局

Wound Closure

时间窗: 12 Weeks

Complete wound closure, defined as 100% epithelialization without drainage.

次要结局

  • Duration of Wound Closure(This is dependent on the time the wound closes, 12 - 20 week estimate.)
  • Wound Area Reduction(12 Weeks)
  • Adverse Events(12 Weeks)
  • Numerical Pain Assessment(12 Weeks)
  • Visual Analogue Pain Assessment(12 Weeks)

研究者

发起方
Bardia Anvar
申办方类型
Industry
责任方
Sponsor Investigator
主要研究者

Bardia Anvar

Principle Investigator

Carbon Life Sciences

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