Burn Clinical Trial
Official title:
A Randomized, Controlled, Prospective Clinical Trial on the Key Technology of Burn Wound Treatment
Verified date | June 2018 |
Source | Xijing Hospital |
Contact | Hu Dahai, Doctor |
Phone | 029-84775293 |
hudhai[@]fmmu.edu.cn | |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Burns are common injuries in the daily life and wars. With the development of medical techniques, the mortality has been significantly reduced. However, the deformity and disability caused by hypertrophic scar have not been improved effectively since the wound repair technology is limited and controversial, especially on the early treatment of deep second degree burns. The prognosis of burns is of great difference. In recent years, the promotion of wound repairing technologies provides a new opportunity for improving the quality of wound healing and solving the problem of scar formation. Although some new methods and techniques have shown significant efficacy in clinic, clinical researches with large samples conducted in multiple centers are still deficient, impeding the evaluation of their superiority. Therefore, the current protocol focuses on the repair of deep second degree burns based on previous researches. There are four types of treatment protocols for wounds. Patients were divided into four groups randomly, including regular dressing change group, controlled debridement + biological dressing covering group (xenogeneic acellular dermal matrix), controlled debridement + epidermal cell cultivation group, controlled debridement + bFGF treatment group. The wound healing rate, healing time and scar formation were observed. The availability and security were evaluated. Further more, treatment guidelines and expert consensuses on deep second degree burn wounds were concluded. Above studies are important to promote the treatment of deep second degree burns to be scientific, standardized and professional in China.
Status | Not yet recruiting |
Enrollment | 200 |
Est. completion date | September 30, 2019 |
Est. primary completion date | December 31, 2018 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 60 Years |
Eligibility |
Inclusion Criteria: 1. Area of deep second burn wound >=10cm×10cm,total burn area =50% TBSA. 2. Within 96 hours after burns and could be managed within 24 hours after included. 3. Ages from 18 to 60. 4. No serious breathing, circulation and other systemic diseases, no surgical contraindications. 5. Agrees to participate in this trial and has signed an informed consent form. Exclusion Criteria: 1. Have severe inhalation injury or shock, or acute respiratory failure; 2. There are serious heart (especially the recent myocardial infarction, myocardial damage, etc.), brain, liver, kidney, lung and other organ disease; 3. Susceptible to allergies; 4. Islamic believers 5. Pregnant women 6. Other cases that are not suitable for study |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Xijing Hospital | Beijing Jishuitan Hospital, First Hospitals affiliated to the China PLA General Hospital, Ruijin Hospital, Second Affiliated Hospital, School of Medicine, Zhejiang University, Southwest Hospital, China, Xiangya Hospital of Central South University |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Wound healing time | Healing time is the number of days when the wound healed completely after management. | 21 days after treatment | |
Secondary | Wound healing rate | Wound healing rate =(area before management - area after management)/ area before management×100%. | 21 days after treatment | |
Secondary | Scar formation | Vancouver scar score | 6 months after treatment |
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