Bedsore. Decubitus ulcer
Conditions
Interventions
Intervention 1: Angipars 4 cc daily, IV for 8 weeks, irrigation with normal saline was performed before and then strile dressing was done. Intervention 2: Normal saline, 4 cc daily IV as placebo for A
Treatment - Drugs
Placebo
Angipars 4 cc daily, IV for 8 weeks, irrigation with normal saline was performed before and then strile dressing was done
Normal saline, 4 cc daily IV as placebo for Angipars for 8 weeks, irrigation with normal saline was performed before and then strile dressing was done
Sponsors
Pars Roos Biotechnology Company
Eligibility
Sex/Gender
All
Age
18 Years to 149 Years
Inclusion criteria
Inclusion criteria: Inclusion criteria: Age more than 18 years, presence of bedsore following spinal injury, lower extremities amputation, chronic diseases such as cerebrovascular attacks, or fracture, wound size at least 1 square centimeter, duration of wound at least 2 weeks, signing written informed consent. Exclusion criteria: Presence of active infection or exposed bone, presence of any concurrent disease which interferes with wound healing such as cancer, vasculitis, diabetes, connective tissue disorder, immune insufficiency, alcohol and drug abuse, dialysis or chronic renal failure, hepatic failure, corticosteroids or immunosuppressive drugs, radiotherapy, chemotherapy, any drug hypersensitivity
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Wound size. Timepoint: Baseline, at the end. Method of measurement: In square centimeter, using ruler. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactDr Kourosh Kamali
Avicenna Research institute
Outcome results
None listed