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Hypertrophic Scar clinical trials

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NCT ID: NCT04012099 Terminated - Hypertrophic Scar Clinical Trials

the Hypertrophic Scar Prevention of BMT101.

Start date: August 21, 2019
Phase: Phase 2
Study type: Interventional

An Independent Evaluator-Blind, Dose-Escalation, Untreated-Controlled, Within-Subject, Phase 2a Therapeutic Exploratory Clinical Trial

NCT ID: NCT03935594 Terminated - Hypertrophic Scar Clinical Trials

Use of Autologous Platelet-Rich Plasma to Treat Hypertrophic Burn Scars

Start date: September 18, 2020
Phase: Phase 2
Study type: Interventional

Hypertrophic burn scars are experienced by more than 70% of burn victims. They are a major source of decreased quality of life in burn patients due to pain, decreased range of motion, and poor cosmetic appearance. Current treatment strategies (including fat grafting and laser resurfacing) are either highly invasive, prohibitively costly, or painful. Autologous Platelet Rich Plasma (PRP) does not require anesthesia, and is an inexpensive, safe, fast, and less painful alternative that has been recognized for its role in reducing scars associated with acne, among other things. While PRP has not been studied specifically in burn scars, there is sufficient theoretical and practical evidence that it will improve the appearance and feel of these debilitating scars, representing a large potential benefit for these patients with minimal associated risk.

NCT ID: NCT03403621 Terminated - Hypertrophic Scar Clinical Trials

Hypertrophic Scar Prevention by Novel Topical Gel Application

Start date: March 5, 2018
Phase: Phase 1/Phase 2
Study type: Interventional

Researchers are trying to find out more about the side effects of topical (applied to the skin) Pentamidine, to determine if it is safe for use in people. They also want to find out if topical use of Pentamidine can help treat hypertrophic scars. Pentamidine is a medicine that is currently used to treat certain kinds of infection. It is most often given by intravenous (into a vein) or inhalation (through a breathing device). This medication is approved by the U.S. Food and Drug Administration (FDA) for use in these forms. Everyone in this study will receive topical Pentamidine (TP) in a silicone based gel (PCCA Pracasil Plus). Topical treatment of Pentamidine is still experimental and has not been formally tested for safety or effectiveness in a randomized control trial within the United States. The FDA has allowed the use of topical Pentamidine in this research study.