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NCT Number: NCT07583862

The Effects of Timolol On Healing and Cosmesis of Mohs Scalp Wounds: An Open Label Trial

The goal of this study clinical trial is to learn if topical timolol can accelerate healing and improve the cosmetic appearance of surgical wounds on the scalp following Mohs surgery. It will include Geisinger patients 18 year or older who undergo Mohs surgery of the scalp with planned wound healing by secondary intent. The main questions in aim to answer are:

1. Compare wound healing speed between patients treated with topical timolol and those receiving standard wound care only. 2. Compare cosmetic outcomes using topical timolol and standard wound care. 3. Evaluate the impact of topical timolol on the number of unplanned follow-up visits and calls related to delayed wound healing.

Participants will be asked use either topical timolol or use standard wound care to treat their Mohs surgery scalp wound. They will follow-up around 4, 8 and 12 weeks.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

About this study

Mohs surgical wounds of the scalp and anterior lower leg share several characteristics. They both involve convex surfaces with high tissue tension, and both are often allowed to heal by secondary intent. Secondary intent healing on the scalp is a slow process, with studies noting a mean time for re-epithelialization ranging from 7 to 26 weeks, depending on if the periosteum is intact.

Recently, topical timolol has garnered attention for its effectiveness in promoting healing of open wounds on the lower extremity. Studies have shown improved healing in patients with comorbidities, an impressive safety profile, and improved cosmesis in wounds healing by secondary intent.5 To our knowledge, no study to date has sought to evaluate the effect of topical timolol on surgical wounds of the scalp.

The study population will be patients at our institution who have undergone Mohs surgery and for whom secondary intent healing ("granulation") is deemed an appropriate treatment.

Endpoints will include time to re-epithelialization, percentage change in wound area, and cosmesis (measured using VAS) at pre-determined follow up intervals.

The potential contribution of this research is to provide evidence on the efficacy and safety of topical timolol in accelerating healing and improving the cosmetic appearance of surgical wounds on the scalp.

We anticipate that timolol will speed wound healing and improve cosmesis of scalp wounds, just as it has in other surgical and non-surgical granulating wounds. The benefits of faster healing and improved cosmesis to individual patients are obvious.

This study may also positively impact health care providers and the health care system, as we anticipate those with faster healing wounds will need fewer follow-up visits and make fewer calls for non-healing wounds.

The affordability of topical timolol could make effective wound care more accessible to a broader range of patients, potentially reducing overall healthcare costs associated with prolonged wound healing and complications. In the future, timolol may be used instead of expensive surgical procedures, allografts, xenografts, and other expensive grafting materials. This cost reduction is also anticipated to benefit health systems.

We anticipate that other institutions will adopt the use of topical timolol for Mohs wounds of the scalp, and that eventually this may become the new standard of care.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Age: Adults aged 18 years and older. Condition: Patients who have undergone Mohs surgery on the scalp. Consent: Ability to provide informed consent. Willingness to Participate: Willingness to comply with study procedures and attend follow-up visits.

Healing by Secondary Intention: Wounds intended to heal by secondary intention.

Exclusion criteria

  • Known allergy or sensitivity to timolol or any components of the study medication.
  • Bronchial asthma or history of bronchial asthma
  • Severe chronic obstructive pulmonary disease (COPD)
  • Sinus bradycardia
  • Second or third-degree atrioventricular block
  • Overt heart failure
  • Cardiogenic shock
  • Under the influence of opioids or benzodiazepines at time of enrollment
  • History of scarring alopecia in area of Mohs wound
  • History of radiation treatment
  • Patients being treated for recurrent tumors

Treatment and study plan

Topical Timolol

Drug

Topical timolol is the active drug that will be compared to placebo in the trial.

normal saline

Drug

Normal saline is the placebo that will be compared to topical timolol in the trial.

Primary outcomes

  1. Healing At 12 Weeks

    Time frame: From treatment start to follow up 12 weeks later

    Percentage of patients achieving complete re-epithelialization at 12 weeks

  2. Scar Cosmesis

    Time frame: Calculated at 4, 8, and 12 week follow up after treatment start.

    Scar cosmesis calculated using visual analog scale (VAS)

Secondary outcomes

  1. Healing At 8 Weeks

    Time frame: From treatment start to follow up 8 weeks later

    Percentage of patients achieving complete re-epithelialization at 8 weeks

  2. Healing At 4 Weeks

    Time frame: From treatment start to follow up 4 weeks later

    Percentage of patients achieving complete re-epithelialization at 4 weeks

  3. Change In Wound Area at Follow Up

    Time frame: Calculated at 4, 8, and 12 week follow up after treatment start.

    Percentage change in overall wound area at specified follow up windows.

  4. Calls for Non-healing Wounds

    Time frame: From treatment start to 12 weeks.

    The number of calls made to our clinic for non-healing wounds or other wound related concerns.

  5. Visits for Non-healing Wounds

    Time frame: From treatment start to 12 weeks.

    The number of visits (other than planned follow up) made to our clinic for non-healing wounds or other wound related concerns.

Study contacts

Contact information is provided by the study sponsor or research team.

Amrit Greene, MD

CONTACT

[email protected]

570-271-8050

Michael Woodfin, MD

CONTACT

[email protected]

570-271-8050

Sponsors and collaborators

Lead sponsor

Geisinger Clinic

Other

Registry information

Important dates

Study start
2026
Primary completion
2028
Study completion
2029
First posted
May 13, 2026
Registry last updated
May 13, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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