Effects of supplementation in the treatment of diabetic foot
Phase 3
- Conditions
- Diabetic foot.With peripheral circulatory complicationsE14.5
- Registration Number
- IRCT201506215623N46
- Lead Sponsor
- Kashan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 60
Inclusion Criteria
Patients with diabetic foot according to Wagner criteria higher than 5 years of their disease; aged 40 to 85 years
Exclusion Criteria
The use of substitute treatments including hormone or vitamin or zinc supplements
Patients with chronic kidney disease, liver, lung, chronic or acute inflammatory diseases, heart valve disease, short bowel syndrome and allergies
Patients with low immune system ability (autoimmune)
Pregnant
Lactating
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Insulin. Timepoint: At the beginning of the study and after 12 weeks of intervention. Method of measurement: Elisa kit.;Insulin resistance. Timepoint: At the beginning of the study and after 12 weeks of intervention. Method of measurement: Calculation using HOMA formula.;Healing of diabetic foot ulcer. Timepoint: At the beginning of the study and after 12 weeks of intervention. Method of measurement: Decrease of the wound size relative to original size: ulcer length (cm), ulcer width (cm), Ulcer depth (cm).
- Secondary Outcome Measures
Name Time Method