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临床试验/NCT06853210
NCT06853210已完成不适用

Treatment of Pressure Ulcers Using Biological Skin Substitutes: A Comparison of High Purity Type-I Collagen and Amnion/Chorion Membranes

Adichunchanagiri Institute of Medical Sciences, B G Nagara2 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2025年3月1日最近更新:

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
80
试验地点
2
主要终点
Percent Change in Wound Area

研究概览

简要总结

Pressure ulcers, also known as decubitus ulcers or bedsores, are localized injuries to the skin and underlying tissue resulting from prolonged pressure. Management of pressure sores is crucial due to their association with increased morbidity, healthcare costs, and reduced quality of life. This study aims to evaluate the efficacy of two treatment modalities: Type-I Collagen-based Skin Substitute (HPTC) vs. Dehydrated Human Amnion/Chorion Membrane (dHCAM)

详细描述

Pressure ulcers, also known as decubitus ulcers or bedsores, are localized injuries to the skin and underlying tissue resulting from prolonged pressure. They are prevalent in individuals with limited mobility, such as the elderly and those with spinal cord injuries, particularly in long-term care settings. Effective management of pressure ulcers is crucial to prevent complications and improve patient outcomes, includes pressure relief, wound care, and advanced therapies such as bioengineered skin substitutes. Management of pressure sores is crucial due to their association with increased morbidity, healthcare costs, and reduced quality of life. This study aims to evaluate the efficacy of two treatment modalities: Type-I Collagen-based Skin Substitute (HPTC) vs. Dehydrated Human Amnion/Chorion Membrane (dHCAM) in promoting the healing of pressure ulcers. While both products are used in wound management, direct comparative studies evaluating their efficacy in treating pressure ulcers are limited.

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
None

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Subjects must be at least 18 years of age or older
  • Presence of a Stage II or Stage III pressure ulcer, as defined by the National Pressure Ulcer Advisory Panel
  • Ulcer size between 5 cm² and 25 cm²
  • Ulcer duration of at least 4 weeks prior to enrollment
  • The subject must agree to attend the twice-weekly/weekly study visits required by the protocol
  • The subject must be willing and able to participate in the informed consent process
  • Adequate blood supply to the affected area, confirmed by clinical assessment

排除标准

  • A subject known to have a life expectancy of <6 months
  • Presence of infection in the ulcer requiring systemic antibiotics.
  • Known allergy to components of HPTC or dHCAM.
  • Participation in another wound care study within the last 30 days.
  • A subject with autoimmune or connective tissue disorders.
  • Women who are pregnant or considering becoming pregnant within the next 6 months and those who are breast feeding.
  • History of autoimmune disease, immunosuppressive therapy, malignancy, or uncontrolled diabetes (HbA1c >10%)

结局指标

主要结局

Percent Change in Wound Area

时间窗: 7 weeks

Percent Change in Wound Area from week 1 through week 7 measured manually with digital photography

Histopathological Parameters - Vascular Infiltration

时间窗: Baseline (Day 0), Day 5

A 2mm punch biopsy was obtained from the wound edge extending into the wound bed under local anaesthesia. Serial sections of 4μm thickness were prepared and stained with Hematoxylin and Eosin (H\&E) for general morphology. Vascular Infiltration: Assessed by counting new blood vessels per High Power Field (hpf) (0-3 scale) 0: Minimal vascular ingrowth (\<5 vessels/hpf) 1. Mild infiltration (5-10 vessels/hpf) 2. Moderate infiltration (11-20 vessels/hpf) 3. Abundant infiltration (\>20 vessels/hpf) (0-worse; 3-better)

Histopathological Parameters - Neo-epithelialization

时间窗: Baseline (Day 0), Day 5

A 2mm punch biopsy was obtained from the wound edge extending into the wound bed under local anaesthesia. Serial sections of 4μm thickness were prepared and stained with: Hematoxylin and Eosin (H\&E) for general morphology. Neo-epithelialization: Measured as epithelial migration distance from wound edge (0-3 scale) 0: No epithelial migration 1. Minimal migration (\<25% wound coverage) 2. Moderate migration (25-75% coverage) 3. Extensive migration (\>75% coverage) (0-worse; 3-better)

Histopathological Parameters - Fibroblast Activity

时间窗: Baseline (Day 0), Day 5

A 2mm punch biopsy was obtained from the wound edge extending into the wound bed under local anaesthesia. Serial sections of 4μm thickness were prepared and stained with: α-SMA immunohistochemistry for fibroblast activity. Fibroblast Activity: Quantified by counting α-SMA positive fibroblasts per HPF and assessment of fibroblast morphology (0-3 scale) 0: Sparse, inactive fibroblasts 1. Moderate cellularity, minimal matrix production 2. High cellularity, active-matrix synthesis 3. Very high activity with extensive matrix deposition (0-worse; 3-better)

Histopathological Parameters - Inflammatory Response

时间窗: Baseline (Day 0), Day 5

2mm punch biopsy was obtained from the wound edge extending into the wound bed under local anaesthesia. Serial sections of 4μm thickness were prepared and stained with: Hematoxylin and Eosin (H\&E) for general morphology Inflammatory Response: Graded semi-quantitatively (0-3 scale) 0: Minimal inflammatory infiltrate 1. Mild chronic inflammation 2. Moderate mixed inflammation 3. Severe acute inflammation (0-better; 3-worse)

Histopathological Parameters - Capillary Density

时间窗: Baseline (Day 0), Day 5

A 2mm punch biopsy was obtained from the wound edge extending into the wound bed under local anaesthesia. Serial sections of 4μm thickness were prepared and stained with: CD31 immunohistochemistry for capillary density evaluation Capillary Density: Evaluated using CD31 staining, counted as vessels per mm² of tissue More the vessels per square centimeters better

Histopathological Parameters - Collagen Deposition

时间窗: Baseline (Day 0), Day 5

A 2mm punch biopsy was obtained from the wound edge extending into the wound bed under local anaesthesia. Serial sections of 4μm thickness were prepared and stained with: Masson's Trichrome for collagen assessment Collagen Deposition: Assessed using Masson's Trichrome staining (0-3 scale) 0: Minimal collagen matrix 1. Loose, immature collagen 2. Moderate organized collagen 3. Dense, mature collagen architecture (0-worse; 3-better)

次要结局

  • Complete Wound Closure Rates(7 weeks)
  • Wound Size Progression Over Time(6 weeks)
  • Mean Number of Repeated Application(6 weeks)
  • Adverse Events(6 weeks)
  • Patient Treatment Satisfaction(7 weeks)

研究者

发起方
Adichunchanagiri Institute of Medical Sciences, B G Nagara
申办方类型
Other
责任方
Principal Investigator
主要研究者

Dr Naveen Narayan MS, MCh (Plastic Surgery)

Professor and HOD

Adichunchanagiri Institute of Medical Sciences, B G Nagara

研究点 (2)

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