Topical 0.5% Timolol Solution for Healing Lower Extremity Wounds
Study Phase: Phase 1
Recruitment Status: Recruiting
Start Date: January 03, 2025
End Date: April 01, 2026
Inclusion Criteria:
- Be scheduled to undergo MMS at 234 East 85th St for a skin cancer that is deemed Mohs
- Appropriate by the Mohs surgery appropriate use criteria
- Have an open surgical wound < 4 cm and > 0.5 cm
- Be ≥18 years of age
- English-speaking
- Provide a signed and dated informed consent form
- State willingness to comply with all study procedures
Exclusion Criteria:
- Age less than 18 years of age
- Open surgical wound > 4 cm
- If tumor clearance cannot be achieved with MMS
- Pregnant women
- Breastfeeding women
- Patients who are taking oral beta-blockers (ie oral timolol, metoprolol, carvedilol, propranolol, atenolol)
- Patients who are currently taking any of the following medications: clonidine, digoxin, methyldopa, quinidine, fluoxetine and paroxetine, bupropion
- Patient currently taking a calcium channel blocker AND has pre-existing heart failure as defined by a reduced ejection fraction
- Patients with pre-existing hypotension
- Pre-existing diagnosis of sinus bradycardia
- Pre-existing diagnosis of second or third degree atrioventricular block
- Congestive heart failure
- Pre-existing diagnosis of severe asthma
- Pre-existing diagnosis of chronic obstructive pulmonary disease
- Any known hypersensitivity to 0.5% timolol solution
- Patients who have a wound where primary closure is feasible and desired by the patient
- Defect size <0.5 cm
- Prior sensitivity or known allergy to timolol
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Conditions:
- Wounds and Injuries