Wound Management

4

Review clinical trials related to Wound Management. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Evaluating Autologous Platelet-Rich Fibrin Plasma for Chronic Lower Extremity Ulcers

To prospectively evaluate the safety and efficacy of an Autologous Platelet-Rich Fibrin Plasma system when applied in conjunction with Standard of Care for management of chronic lower extremity wounds.

Participants needed: 30
Trial details
Phase: Phase 1, Phase 2Age: 18+Biological sex: AllType: InterventionalSponsor: Tiger Biosciences, LLC.Updated: Oct 7, 2026
Eligibility criteria

Female or Male, plus ≥18 years of age at the time the study Informed Consent is... [+13]

Ulcer is not medically diagnosed as a lower extremity wound. [+25]

Status: Not yet recruiting

Evaluating Autologous Platelet-Rich Fibrin Plasma for Chronic Diabetic Foot Ulcers

To prospectively evaluate the safety and efficacy of an Autologous Platelet-Rich Fibrin Plasma system when applied in conjunction with Standard of Care for management of chronic Diabetic Foot Ulcers.

Participants needed: 55
Trial details
Phase: Phase 1, Phase 2Age: 18+Biological sex: AllType: InterventionalSponsor: Tiger Biosciences, LLC.Updated: Sep 25, 2026
Eligibility criteria

Female or Male, plus ≥18 years of age at the time the study Informed Consent is... [+17]

Ulcer is not medically diagnosed as DFU pathophysiology. [+28]

Status: Not yet recruiting

Urinary Bladder Matrix (UBM) Registry

The purpose of this registry is to collect real-world information on patients treated with Urinary Bladder Matrix (UBM) products. The study will evaluate patient characteristics, treatment patterns, and clinical outcomes to better understand how UBM products are used in routine clinical practice and the outcomes experienced by patients over time.

Participants needed: 300
Trial details
Age: 21+Biological sex: AllType: ObservationalSponsor: Integra LifeSciences CorporationUpdated: Sep 4, 2026Duration: 12 Months
Eligibility criteria

Adults aged ≥21 years at the time of initial urinary bladder matrix (UBM) produc... [+2]

Wound treated with a skin substitute prior to UBM treatment. [+4]

Status: Not yet recruiting

"Ultrasound-Enhanced Propolis Therapy for Healing Diabetic Foot Wounds"

This study aims to evaluate whether using ultrasound (phonophoresis) can help deliver propolis-a natural compound made by bees-more effectively into the skin to speed up wound healing in people with diabetic foot ulcers. Diabetic foot ulcers are a common and serious complication of diabetes and often take a long time to heal. Propolis has natural anti-inflammatory and antimicrobial properties that may promote healing, but it does not easily penetrate the skin. By using ultrasound to enhance absorption, this study tests whether combining propolis with phonophoresis is more effective than standard wound care alone. Participants will be randomly assigned to receive either the propolis ultrasound therapy or standard care. The study will measure wound size, healing time, pain, infection rates, and quality of life.

Participants needed: 80
Trial details
Age: 18-75Biological sex: AllType: InterventionalSponsor: Sinai UniversityUpdated: Aug 4, 2026
Eligibility criteria

Not listed