Plasma Therapy for Diverse Wounds
Starting soon
Conditions studied: Wound Care
In brief
This study is a prospective, multicenter, real-world observational study. It aims to evaluate whether adding plasma device therapy to standard wound care is effective and safe for treating different types of wounds, including acute wounds (such as burns and surgical incisions), chronic wounds (such as diabetic foot ulcers and pressure injuries), post-grafting wounds, and sutured wounds. A total of 500 patients receiving standard wound care plus plasma therapy will be enrolled from multiple hospitals across China. Their outcomes will be compared with 500 matched patients who received standard wound care alone. The main outcomes include wound healing rate at 4 weeks, time to complete wound closure, pain relief, scar formation, and any side effects. Patients will be followed for up to 6 months.
Key facts
- Study ID
- NCT07553689
- Run by
- First Affiliated Hospital, Sun Yat-Sen University
- People needed
- 1000
- Starts
- 2026-05-01
- Expected to finish
- 2029-12-31
- Last updated by the study team
- 2026-04-28
Who can join
Age: any. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Presence of any of the following wound types: acute wounds (burns, trauma, surgical incisions, skin avulsions), chronic wounds (diabetic foot ulcers, pressure injuries, venous ulcers, radiation ulcers, burn residual wounds), post-grafting wounds (autograft or allograft, including donor and recipient sites), or sutured wounds (postoperative incisions, flap surgery, tension-reducing sutures).
- Age ≥ 12 years (for minors under 18 years, informed consent must be provided by a parent or legal guardian).
- Stable vital signs and able to tolerate wound treatment.
- Willing to participate and able to provide signed informed consent.
You may not qualify if…
- Active malignant tumor involving the wound area.
- Severe systemic infection or sepsis.
- Severe immunodeficiency or long-term use of high-dose corticosteroids.
- Intolerance to plasma therapy or refusal to participate.
- Pregnancy or breastfeeding.
Full record on ClinicalTrials.gov
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