CHU Amiens
Amiens, 80054, France
NCT Number: NCT02422017
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.
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Notify Me18 year and older
All sexes
Interventional
Phase 2
Amiens, 80054, France
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.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Patients will receive one drop of timolol every 6cm ² every other day for twelve weeks applied on the ulcer of interest
Other names: Timoptol
Local care treatment with dressing compression in accordance with standards applied every other day
Time frame: 12 weeks
Assess the healing rate in patients treated with topical timolol associated with wound dressing and compression for 12 weeks, compared to patients treated with wound dressing and compression.
Success is defined as an ulcer surface relative reduction >= 40%
Time frame: 12 weeks
Complete healing of the ulcer i.e. 100% regression of the ulcer surface and replaced by an epidermised tissue.
Time frame: 12 weeks
To assess local and cardiac safety of timolol by cardiac-related serious adverse events evaluation
Time frame: Baseline and 12 weeks
Evaluation of the quality of life of patients by the Dermatology Life Quality Index (DLQI) scale at baseline and after 12 weeks of treatment
Centre Hospitalier Universitaire, Amiens
Other
Acronym: EETUV
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