Eye drop gel shows promise for skin graft healing, but trial stalls
NCT ID NCT03579160
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 2 times
Summary
This study tested whether applying 0.25% timolol gel (a beta-blocker eye drop used for glaucoma) to skin grafts could improve healing and appearance after skin cancer surgery. Researchers planned to enroll 82 patients but stopped early with only 10 participants. The goal was to see if the gel helps wounds heal faster and look better compared to standard Vaseline dressing.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- 0.25% timolol gel
- What this could lead to
- If it works, this could offer a simple, low-cost way to improve healing and cosmetic outcomes for skin grafts after cancer surgery.
- What could go wrong
- The trial was terminated early with only 10 participants, so results are very limited. It is unclear if timolol gel is truly effective or safe for this use.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Phase 2/3
Runs two stages together: whether the treatment works, then large-scale confirmation.
- Participants
-
10 people
The number who actually took part.
- Started
-
Jan 2019
- Finished
-
Jan 2022
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
18 years and older
- Sex
-
Anyone
- Healthy volunteers
-
Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
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
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Genom att skicka in godkänner du våra Användarvillkor
Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Mohs and Dermatologic Surgery Center, Brigham and Women's Hospital
Boston, Massachusetts, 02130, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Can a DNA vaccine teach the immune system to hunt melanoma?
- Can a simple ointment make surgical scars heal better?
- Can a workplace campaign shade outdoor workers from skin cancer?
- Can a dissolvable dressing get burn patients to skin grafts faster?
- Could a special dressing make skin grafts unnecessary for burns?
- Can tiny skin grafts heal wounds without leaving a second scar?