Topical Timolol: a Comparison of Surgical Outcomes

Keith G. LeBlanc, Jr, MD

Status and phase: Unknown; Phase 2

Conditions: Wound Heal

Treatments: Drug: Timolol 0.25% Ophthalmic Solution; Other: Standard Wound Care

Study type: Interventional

Funder types: Other

Identifiers

NCT05114239

1227

Details and patient eligibility

About

The use of topical beta-blockers, such as 0.25% timolol, in promoting wound healing is currently emerging in the literature. The investigators will enroll 30 participants in a split scar study who have their skin cancer surgically removed resulting in a linear wound equal to or longer than 4cm. The objective of this randomized study is to determine the safety and efficacy of 0.25% timolol in promoting wound healing in wound closed primarily greater than or equal to 1.5 cm.

Full description

Topical timolol has shown in case series to improve healing time and cosmetic outcome of ulcerated or non-healing wounds with improved cosmetic outcome when compared to standard wound care. There is currently no research detailing if this improved outcome is applicable when used with wounds approximated with sutures.

Mechanism of action is not fully elucidated but improved keratinocyte migration and suppression of the inflammatory cascade is thought to improve wound healing. Skin cancer surgeries have morbidity for patients as they are often in cosmetically sensitive locations. Improving cosmetic outcomes of surgical scars could improve patient outcomes and overall satisfaction.

The goal of this study is to determine if topical timolol will improve long-term cosmetic outcomes of surgical scars and thereby improve patient outcomes. There is great variability in how a surgical site heals depending on patient factors as well as surgical site location. The investigators will perform a split scar study to allow each patient to be their own control to account for this variability.

To assess the efficacy and safety of topically applied 0.25% timolol in promoting wound healing in surgical primary linear wound greater than or equal to 4cm versus standard of care (SOC) by:

1. Evaluating cosmetic outcomes of surgical wounds in terms of blinded physician and patient assessment at 30 days and 90days following suture removal
2. Evaluating patient discomfort by patient questionnaire.
3. Determining the side effects associated to 0.25% topical timolol versus SOC;

Enrollment: 30 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• skin wounds greater than or equal to 4cm, closed primarily and linearly following standard excision or Mohs

Exclusion criteria

• Past medical history of psoriasis
• known history of sensitivity to beta blockers or topical timolol
• pregnant women

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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30 participants in 2 patient groups, including a placebo group

Timolol

Experimental group

Description:

Timolol 0.25% applied to distal or posterior half of wound edge twice daily prior and adjunct to prior wound care.

Treatment:

Drug: Timolol 0.25% Ophthalmic Solution

Standard Wound Care

Placebo Comparator group

Description:

Petrolatum ointment

Treatment:

Other: Standard Wound Care