Clinical Trial

Comparison of Pain Reduction in Painful Chronic Wounds With and Without Fat Grafting

Study acronym: PAINFAT
Not Yet Recruiting
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Record status
This record was last updated March 18, 2026 (before its estimated May 1, 2026 completion). Its status may not reflect the trial's current state.
Summary
Chronic wounds, such as those caused by diabetes, burns, or poor blood circulation, often heal slowly and can cause significant pain, affecting daily life and quality of life. This study aims to evaluate whether autologous fat grafting-a procedure in which a patient's own fat tissue is injected into the wound-can reduce pain and improve healing in chronic wounds compared to standard care without fat grafting. We will enroll 62 adult patients with chronic wounds lasting more than 3 months. Participants will be randomly assigned to two groups: one group will receive fat grafting along with standard wound care, and the other group will receive standard wound care alone. Pain will be measured using a Visual Analog Scale (VAS) over 21 days after treatment. Wound healing and any complications will also be monitored. The results of this study will help determine if autologous fat grafting is an effective and safe method to reduce pain and improve recovery in patients with chronic wounds.
Trial Details
NCT Number NCT07480447
Lead Sponsor King Edward Medical University
Conditions Wound and Injuries, Pain
Enrollment 62 participants
Start Date 2026-05-01
Primary Completion 2026-05-01 (estimated)
Study Completion 2026-11-01 (estimated)
Updated on ClinicalTrials.gov 2026-03-18