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Beta Blocker

Timolol for Diabetic Foot Ulcers (BAART-DFU Trial)

Phase 3
Waitlist Available
Led By Sara E. Dahle, DPM MPH
Research Sponsored by VA Office of Research and Development
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Must not have
Female who is pregnant or refuses to use adequate contraceptive methods and is of childbearing age during the trial
Ulcer of non-diabetic etiology, such as venous, arterial and burn wounds
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 31 weeks
Awards & highlights

Summary

This trial is testing if timolol, an eye drop medicine, can help heal diabetic foot ulcers. The study focuses on Veterans with these ulcers because they are hard to treat and can lead to amputations. Timolol might help wounds heal faster when applied directly to them.

Who is the study for?
Adults with diabetic foot ulcers that are between 0.5cm2 and 20cm2 in size, have lasted more than 30 days but less than 2 years, and have an Ankle Brachial Index within a specific range can join this trial. People cannot participate if they've abused drugs recently, are pregnant without contraception use, have certain infections or immune deficiencies, received recent ulcer treatments like skin grafts or growth factors, or suffer from severe malnutrition.
What is being tested?
The study is testing the effectiveness of timolol—a medication typically used as eye drops for glaucoma—applied directly to diabetic foot ulcers compared to a placebo gel. Participants will be randomly assigned to either receive the standard care plus timolol or standard care plus the non-active gel.
What are the potential side effects?
Timolol may cause side effects such as fatigue, palpitations (feeling your heartbeat), shortness of breath (dyspnea), chest pain at rest (angina), and could potentially worsen heart block in those predisposed.

Eligibility Criteria

Exclusion Criteria

You may be eligible for the trial if you check “No” for criteria below:
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I am not pregnant and agree to use birth control during the trial.
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I have a non-diabetic wound like a venous, arterial, or burn wound.
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I have an active cancer on my foot.
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I experience tiredness, heart palpitations, shortness of breath, or chest pain without doing anything.
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My study foot has more than 3 ulcers.
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My ulcer shows signs of severe infection or exposed bone.
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My blood protein levels are very low.
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My diabetes is not under control, with an A1C level over 12%.
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I have a history of serious heart rhythm problems.
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My skin ulcer is close to another ulcer on the same limb.
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I haven't had treatments like immunosuppressants or chemotherapy on my ulcer in the last 60 days.
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My wound is infected, as shown by symptoms or tests.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~31 weeks
This trial's timeline: 3 weeks for screening, Varies for treatment, and 31 weeks for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Measurement of timolol serum during the treatment phase
Time to complete wound closure, as assessed over a 12 week period

Side effects data

From 2009 Phase 3 trial • 139 Patients • NCT00716859
6%
Nasopharyngitis
3%
Conjunctival hyperaemia, study eye
3%
Pyrexia
3%
Headache
3%
Rhinitis
1%
Viral infection
1%
Lens dislocation, study eye
1%
Pneumonia viral
1%
Gastroenteritis
1%
Conjunctival hyperaemia, both eyes
1%
Bronchopneumonia
100%
80%
60%
40%
20%
0%
Study treatment Arm
Latanoprost
Timolol

Trial Design

2Treatment groups
Experimental Treatment
Placebo Group
Group I: TimololExperimental Treatment1 Intervention
Timoptic-XE plus standard of care (SOC)
Group II: SOC plus non biologically active gelPlacebo Group1 Intervention
SOC plus non biologically active gel (hydrogel as placebo medication)
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Timolol
2017
Completed Phase 3
~1620

Research Highlights

Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.
Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Common treatments for foot ulcers include debridement, infection control, and advanced wound care therapies such as dressings and skin substitutes. Debridement removes dead tissue to promote healing, while infection control prevents bacterial growth that can impede recovery. Advanced wound care therapies provide a conducive environment for tissue regeneration. Timolol, a beta-adrenergic receptor blocker, is being studied for its potential to promote wound healing by enhancing blood flow and reducing inflammation at the ulcer site. This is significant for foot ulcer patients as improved blood flow and reduced inflammation can accelerate healing and reduce the risk of complications such as infections and amputations.
Prostanoids in patients with peripheral arterial disease: A meta-analysis of placebo-controlled randomized clinical trials.

Find a Location

Who is running the clinical trial?

VA Office of Research and DevelopmentLead Sponsor
1,647 Previous Clinical Trials
3,360,035 Total Patients Enrolled
6 Trials studying Foot Ulcer
1,142 Patients Enrolled for Foot Ulcer
VA Northern California Health Care SystemFED
18 Previous Clinical Trials
3,412 Total Patients Enrolled
1 Trials studying Foot Ulcer
120 Patients Enrolled for Foot Ulcer
Sara E. Dahle, DPM MPHPrincipal InvestigatorVA Northern California Health Care System, Mather, CA

Media Library

Timolol (Beta Blocker) Clinical Trial Eligibility Overview. Trial Name: NCT03282981 — Phase 3
Foot Ulcer Research Study Groups: SOC plus non biologically active gel, Timolol
Foot Ulcer Clinical Trial 2023: Timolol Highlights & Side Effects. Trial Name: NCT03282981 — Phase 3
Timolol (Beta Blocker) 2023 Treatment Timeline for Medical Study. Trial Name: NCT03282981 — Phase 3
~5 spots leftby Sep 2025