Comparative study of the effect of fluoxetine and gabapentin in diabetic foot patients
Phase 3
- Conditions
- Diabetic foot ulcer.Non-pressure chronic ulcer of thighL97.1
- Registration Number
- IRCT20200324046850N4
- Lead Sponsor
- Abadan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- 100
Inclusion Criteria
Inclusion criteria are: at least one year past diagnosis of diabetes, symptoms of neuropathy and tendency to participate in the study, as well as diabetic foot patients with grade 1 (superficial ulcer) and grade 2 (deep tendon ulcer or articular capsule) will be included in the study
Exclusion Criteria
Cases such as patients with concomitant cardiovascular disease, noncompliance with medication and trials, and diabetic foot patients with grade 3 or more ulcer are excluded.
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Severity of pain. Timepoint: On the first days, 15 and 30 examinations. Method of measurement: Pain assessment is done on the first, 15th, and 30th days after intervention based on the VAS index, both verbally and visually.
- Secondary Outcome Measures
Name Time Method