Evaluation of efficacy and side effects of chitosan alginate dressings in chronic wound heal
Phase 2
Recruiting
- Conditions
- Chronic ulcer.Chronic ulcer of skin, not elsewhere classified
- Registration Number
- IRCT2016041927480N1
- Lead Sponsor
- Vice-Chancellor in Research Affairs, Shahid Beheshti University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 32
Inclusion Criteria
age more than 18 years old; chronic wound with duration more than 4-6 weeks; wound diameter 1-200 square centimeter; consent for entering trial.
Exclusion criteria: refuse to enroll; allergy to shellfish, lobster; attending other trials; pregnancy; lactation; severe co-morbidity; collagen vascular ulcers or severe infected ulcers.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method For chronic ulcer assessment of remission. Timepoint: Visit and photo taking each 2-3 days. Method of measurement: 0-24...no improvement,25-49:...moderate improvement,50-74:significant improvement.....75-100:complete improvement.;Degree of erythema. Timepoint: Visit and photo taking each 2-3 days. Method of measurement: 0: no erythema,1:pink,2:red.;Degree of exudate. Timepoint: Visit and photo taking each 2-3 days. Method of measurement: 0:no 1:low 2: moderate-severe.;Degree of odor. Timepoint: Visit and photo taking each 2-3 days. Method of measurement: 0:negative 1:positive.;Patient satisfaction. Timepoint: Visit and photo taking each 2-3 days. Method of measurement: Low noderate good excellent.
- Secondary Outcome Measures
Name Time Method