Diabetic foot ulcer. Non-pressure chronic ulcer of lower limb, not elsewhere classified
Conditions
Interventions
administration of 50000 units of vitamin D per week, together with routine diabetic foot ulcer treatment during the study. Intervention 2: Control group: for patients in the control group
only administration of routine diabetic foot ulcer treatment during the study.
Sponsors
Shahroud University of Medical Sciences
Eligibility
Sex/Gender
All
Age
15 Years to 70 Years
Inclusion criteria
Inclusion criteria: Patients with diabetic foot ulcer Suffering to Type 2 diabetes Satisfaction in rasarach
Exclusion criteria
Exclusion criteria: Pregnancy The presence of autoimmune disease Use of anticonvulsants Antibiotic use in the last two months low blood pressure Osteomyelitis The need for a large debridement Inadequate kidny Skin tumors on the wound Lack of sense in the lower limbs Dissatisfaction in rasarach
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Diabetic foot ulcer area. Timepoint: Before, 4 weeks, 8 weeks and 12 weeks after intervention. Method of measurement: With Auto cad 2010.;Depth of diabetic ulcers. Timepoint: Before, 4 weeks, 8 weeks and 12 weeks after intervention. Method of measurement: ulcers will be evaluated according to University of Texas Foot Wound Classification System. | — |
Secondary
| Measure | Time frame |
|---|---|
| Serum CRP. Timepoint: Before, 4 weeks, 8 weeks and 12 weeks after intervention. Method of measurement: In a quantitative laboratory method.;Serum WBC. Timepoint: Before, 4 weeks, 8 weeks and 12 weeks after intervention. Method of measurement: In laboratory method. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactMohammad Bagher Sohrabi
Shahroud University of Medical Sciences
Outcome results
None listed