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Recruiting NCT05984628

Umbilical Cord Stem Cells for Skin Grafts in Donor Site Wounds

Trial Parameters

Condition Skin Wound
Sponsor Fujian Medical University Union Hospital
Study Type INTERVENTIONAL
Phase N/A
Enrollment 88
Sex ALL
Min Age 18 Years
Max Age 60 Years
Start Date 2021-10-20
Completion 2025-09-01
Interventions
human umbilical cord mesenchymal stem cellsblank solvent

Brief Summary

The goal of this clinical trial is to evaluate the safety and effectiveness of human umbilical cord mesenchymal stem cell (hUCMSC) therapy in patients undergoing medium-thickness skin grafts for donor site wounds. The study aims to answer the following main questions: * Question 1: Does hUCMSC therapy improve the healing quality and speed of donor site wounds in comparison to standard treatment? * Question 2: Does hUCMSC therapy reduce scar formation in the donor site wounds? Participants in this study will undergo medium-thickness skin grafts, and those in the treatment group will receive hUCMSC therapy. The main tasks for participants will involve regular follow-up visits, monitoring of wound healing progress, and assessment of any potential side effects or complications associated with the therapy. In order to evaluate the effectiveness of hUCMSC therapy, researchers will compare the treatment group receiving hUCMSC therapy with a control group that receives standard treatment alone. The aim is to determine if the use of hUCMSC therapy leads to improved healing outcomes and reduced scar formation compared to the standard treatment group.

Eligibility Criteria

Inclusion Criteria: 1. Patients between 18 and 60 years old with extensive scars, large benign tumors, or fresh wounds on the body surface. 2. Patients who undergo medium-thickness skin graft surgery (donor site can be from the thigh, abdomen, or back). 3. Participants who have a thorough understanding of the study objectives, significance, implementation plan, potential benefits, risks involved, measures to address risks, and the rights and obligations of the subjects (including privacy protection and the right to withdraw), and are willing to participate in this clinical study and can cooperate effectively. Exclusion Criteria: Participants who meet any of the following criteria are not suitable for inclusion: 1. Hypertension, hypotension, heart disease (including history of myocardial ischemia, coronary heart disease, myocarditis). 2. Liver or kidney dysfunction. 3. Infectious diseases (including viral hepatitis, syphilis, HIV/AIDS, etc.). 4. Venous thrombosis, thoracic or abdominal

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