Novel Strategies for Reducing Burn Scar Itch

PHASE3RecruitingINTERVENTIONAL
Enrollment

44

Participants

Timeline

Start Date

March 1, 2025

Primary Completion Date

December 31, 2026

Study Completion Date

November 1, 2027

Conditions
Burn ScarItch ScarringWound
Interventions
COMBINATION_PRODUCT

Famotidine and 4% topical cromolyn sodium

Patients will be instructed to take a 20mg famotidine capsule twice daily, and to use the lotion (4% cromolyn sodium) twice daily.

OTHER

Placebo

Treatment with active H1 antihistamine plus administration of placebo famotidine and placebo cromolyn sodium.

Trial Locations (1)

77555

RECRUITING

University of Texas Medical Branch, Galveston, Galveston

All Listed Sponsors
collaborator

University of Texas

OTHER

lead

The University of Texas Medical Branch, Galveston

OTHER