Clinical Trial

Subcutaneous Dexpanthenol Administration and Wound Epithelialization

Study acronym: DEXPAN-WOUND
Not Yet Recruiting
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Summary
Chronic wounds are wounds that do not heal properly over time and can significantly reduce quality of life. Common types include diabetic foot ulcers, venous leg ulcers, and arterial ulcers. Improving wound healing and speeding up skin regeneration (epithelialization) are important goals in the care of these patients. Dexpanthenol is a vitamin B5 derivative that supports skin repair and tissue regeneration. It is widely used in topical treatments, and injectable forms are approved for clinical use. However, the effects of subcutaneous (under the skin) dexpanthenol injections on chronic wound healing have not been sufficiently studied in clinical settings. The purpose of this study is to evaluate whether adding subcutaneous dexpanthenol injections to standard wound care improves wound healing compared with standard wound care alone. Adult patients with non-infected chronic wounds will be randomly assigned to one of two groups. One group will receive standard wound care only, while the other group will receive standard wound care plus subcutaneous dexpanthenol injections around the wound area. Wound healing will be assessed by measuring changes in wound size and the degree of skin epithelialization over time using standardized and objective methods. Safety will be monitored by recording local reactions at the injection site and any other adverse events during the study. The results of this study may provide preliminary clinical evidence on the effectiveness and safety of subcutaneous dexpanthenol as an additional treatment option for chronic wound management.
Protocol Amendment History 2 changes
notable Primary completion pushed: 2026-06-02 -> 2028-08-02 2026-04-22
minor Completion pushed: 2026-07-02 -> 2028-12-02 2026-04-22
Trial Details
NCT Number NCT07395674
Lead Sponsor Dilara CANBAY OZDEMIR
Conditions Chronic Wounds, Diabetic Foot Ulcer, Venous Leg Ulcers, Arterial Ulcer
Enrollment 40 participants
Start Date 2026-08-02
Primary Completion 2028-08-02 (estimated)
Study Completion 2028-12-02 (estimated)
Updated on ClinicalTrials.gov 2026-04-21