Treatment of bedsore
Phase 2
- Conditions
- bedsore.Decubitus ulcer and pressure area
- Registration Number
- IRCT2013072912438N4
- Lead Sponsor
- Barij Essence research center of medicinal herbs
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 102
Inclusion Criteria
All patients with bedsores Exclusion criteria: cardiovascular diseases, malignancies, end-stage disease - systemic or topical antibiotics - taking glucocorticoids and other local and systemic immunosuppressant drugs - other chronic cutaneous illnesses- sensitivity of herbal products-Desire to withdraw from the study.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method ength x Width. Timepoint: end of each week. Method of measurement: greatest lengthx greatest width with ruler.;Exudate amount. Timepoint: end of each week. Method of measurement: observation.;Tissue type. Timepoint: end of each week. Method of measurement: observation.
- Secondary Outcome Measures
Name Time Method