RecruitingBurn ScarItch ScarringWound
Novel Strategies for Reducing Burn Scar Itch
Eligible age
18–80 yrs
Accepts
All genders
Locations
1 state
Healthy volunteers
No
See if you qualify for this study
Answer a few quick questions about your location and health. Takes about a minute.
About this study
The purpose of the study is to see whether using diphenhydramine (Benadryl), famotidine (Pepcid), and cromolyn sodium will decrease burn scar itch.
Sponsor: The University of Texas Medical Branch, Galveston
You may qualify if…
- ✓ 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 \<80 years of age.
- ✓ Has an itchy burn scar.
You may not qualify if…
- ✕ Participants meeting any of the exclusion criteria at baseline will be excluded from study participation.
- ✕ Failure to obtain consent or unable to return for follow up assessments.
- ✕ Patient is unable to follow the protocol required assessments.
- ✕ Member of a vulnerable class (e.g., prisoners, pregnant participant, etc.).
- ✕ Any medical condition that, in the opinion of the investigator or physician, would place the participant at increased risk for participation.
- ✕ Concurrent participation in another interventional clinical trial (to avoid confounding factors that may influence outcomes).
- ✕ History of prior non-compliance or the presence or history of psychiatric condition (including drug or alcohol addiction) that would, in the opinion of the investigator, make it difficult for the participant to comply with the study procedures or follow the investigators instructions.
- ✕ Age \< 18 or ≥ 80 years.
Where it's recruiting
Texas
Galveston
Source: ClinicalTrials.gov · NCT06801626 · last updated 2025-09-24