Overview
Efficacy and Safety of 0.25% Timolol Gel in Enhancing Full Thickness Skin Grafts Healing and Cosmetic Outcomes
Status:
Recruiting
Recruiting
Trial end date:
2022-07-31
2022-07-31
Target enrollment:
0
0
Participant gender:
All
All
Summary
The use of topical beta-blockers, such as 0.25% timolol, in promoting wound healing is currently emerging in the academic literature. The investigators will enroll 82 patients who have their skin cancer surgically removed resulting in the need of a full-thickness skin graft. The objective of this randomized safety study is to determine the safety and efficacy of 0.25% timolol in promoting wound healing in full-thickness skin grafts compared to standard of care.Phase:
Phase 2/Phase 3Accepts Healthy Volunteers?
Accepts Healthy VolunteersDetails
Lead Sponsor:
Brigham and Women's HospitalTreatments:
Petrolatum
Timolol
Criteria
Inclusion Criteria:1. Age ≥18 years of age
2. Undergoing a procedure which results in the need of a FTSG
3. Willing to provide written informed consent
Exclusion Criteria:
1. Age less than 18 years of age
2. Pregnant women
3. (Use of systemic drugs that can impede wound healing, such retinoids or
immune-suppressive drugs)
4. Severe coagulation disorders
5. Severe, uncontrolled systemic comorbidities, such as diabetes, arthritis, etc.
6. Hypersensitivity to 0.25% timolol gel
7. Not willing to provide written informed consent