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Recruiting NCT06801626

Novel Strategies for Reducing Burn Scar Itch

Conditions: Burn Scar, Itch Scarring, Wound

Sex: All

Ages: 18 Years – 80 Years

Healthy volunteers: No

Phase: PHASE3

Enrollment: 44

Sponsor: The University of Texas Medical Branch, Galveston

Location: University of Texas Medical Branch, Galveston Galveston Texas

Summary

The purpose of the study is to see whether using diphenhydramine (Benadryl), famotidine (Pepcid), and cromolyn sodium will decrease burn scar itch.

Eligibility Criteria

Inclusion Criteria: Participants must meet all the inclusion criteria in order to be eligible to participate in the study. * Participant has provided informed consent in a manner approved by the IRB and is willing and able to comply with the trial procedures. * Adults: ≥18 to \

Interested in this study? View the official listing for contact and enrollment details.

View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT06801626). StuddyBuddy aggregates publicly available trial information.