Evaluation of absorbable Dressing containing Red Propolis for use in chronic Wound: clinical study
- Conditions
- Wounds and InjuriesC17.800
- Registration Number
- RBR-10ms8yjv
- Lead Sponsor
- niversidade Federal de Alagoas
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- Not specified
Minimum age of 18 years. Volunteers with chronic venous injury using unna boot compression or elastic therapy. Surface area up to 150 cm2. Wound covered with > 50% granulation tissue, no black necrotic tissue on the wound surface, and spaced > 3cm from any wound edge to another wound located on the same limb. Both genders. Variable nutritional status and hydration. They may carry the most varied clinical pathologies
Hypersensitivity to one of the dressing components, poor health, body mass index (BMI) in the grade 3 obesity range, erysipelas, cellulitis, lymphangitis, chronic lymphedema. Malignant wound degeneration or neoplastic lesion treated by radiotherapy, chemotherapy and immunosuppressive drugs or corticosteroid dose. Clinically infected lesion requiring a systemic antibiotic. History of deep or superficial venous thrombosis in the previous three months. Have undergone surgery directly related to venous insufficiency within two months prior to inclusion. Wound surgery planned during the trial period. Patients who are in the terminal phase will not be included in the study
Study & Design
- Study Type
- Intervention
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method