Topical Timolol Benefit in Venous Ulcers
Information source: Centre Hospitalier Universitaire, Amiens
ClinicalTrials.gov processed this data on August 23, 2015 Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Venous Leg Ulcers
Intervention: Timolol (Drug); Local care treatment (Other)
Phase: Phase 2
Status: Not yet recruiting
Sponsored by: Centre Hospitalier Universitaire, Amiens Overall contact: Catherine LOK-CHARLES, MD, PhD, Phone: 03.22.45.58.41, Email: lok.catherine@chu-amiens.fr
Summary
Background: Venous Leg ulcers are a frequent pathology in dermatology and complex in their
management. At the origin of high health costs and strong repercussions on quality of life
for patients, they require long management and may be subject to possible complications.
In spite of appropriate treatment, 50-60% of these ulcers are not healed at 24 weeks.
Purpose: Topical beta adrenergic antagonists have shown efficacy in wound healing. The
purpose of this study is to evaluate the efficacy and safety of treatment of chronic venous
ulcers with topical timolol.
Clinical Details
Official title: Topical Timolol Benefit in Venous Ulcers
Study design: Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
Primary outcome: Success rate
Secondary outcome: Complete healingTolerance (cardiac-related serious adverse events) Quality of life evolution
Detailed description:
Abstract: Complicating severe stages of chronic venous insufficiency, venous leg ulcers are
common in dermatology and responsible for important health care costs. Healing remains long
with many persistent cases after one year, despite compression and local dressings. Several
pharmacological studies have demonstrated a benefit of beta-blockers on the wound healing
process: present in the skin, the beta-adrenergic receptors play a role in wound healing.
Their stimulation inhibits healing while blocking them promotes angiogenesis, fibroblast
migration and keratinocyte migration. Using the topical timolol in several patients seems to
confirm these effects: all ulcers treated with timolol healed in a few weeks whereas they
did not evolve under local care and compression.
The purpose of this study is to demonstrate whether there is an interest in topical timolol
for venous leg ulcers in combination with compression and wound dressings versus placebo.
The primary endpoint is to evaluate the healing rate to W12. The effects will be evaluated
with photography, evaluation of the surface of the ulcer at W12 compared to W0. The research
of side effects will also be evaluated.
Eligibility
Minimum age: 18 Years.
Maximum age: N/A.
Gender(s): Both.
Criteria:
Inclusion Criteria:
- Affiliated to a social security scheme patients
- Informed consent
- Patients over 18 years
- Ulcer lasting for at least 24 weeks with no improvement observed after 4 weeks of
well conducted treatment (compression and local care)
- Presence of one or more venous leg ulcers (objectified by a Doppler ultrasound dated
within 6 months and ABPI ≥ 0. 8)
- Ulcers with a surface of 5 to 50 cm ² and at granulation stage
- Study ulcer must be at least 2 cm from Any Other ulcer on same extremity.
- If several ulcers present, the greatest is selected
- Granulation tissue ≥ 50%
Exclusion Criteria:
- Minors under guardianship, deprived of liberty, not looking at treatment, lack of
signed consent, pregnant women, demented patients
- Ulcer lasting for less than 24 weeks
- Granulation tissue <50%
- Obliterative arteritis (ABPI <0. 8)
- Infection of the ulcer (need to treat the infection before any inclusion criteria be
compatible)
- Non-cardioselective beta-blocker treatment
- Bradycardiac treatment
- Patients under diltiazem, verapamil (calcium antagonists)
- Reaching underlying noble structures, tumor acutisation wound
- Immunosuppression
- Diabetes unbalanced (HbA1c> 8%)
- Severe Malnutrition (albumin <25g / L)
- Anemia <10g/dl
- Contraindication to beta-blockers
Locations and Contacts
Catherine LOK-CHARLES, MD, PhD, Phone: 03.22.45.58.41, Email: lok.catherine@chu-amiens.fr
CHU Amiens, Amiens 80054, France; Not yet recruiting Catherine LOK-CHARLES, MD, PhD, Phone: +333.22.45.58.41, Email: lok.catherine@chu-amiens.frlok.catherine@chu-amiens.fr Thomas BALTAZARD, Phone: +333.22.45.58.41, Email: thomas.baltazard@gmail.com
Additional Information
Starting date: April 2015
Last updated: April 20, 2015
|