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The evaluation of the effect of pentoxifylline on diabetic foot ulcers

Phase 2
Conditions
Diabetes mellitus.
Diabetes mellitus due to underlying condition
Registration Number
IRCT20180818040823N1
Lead Sponsor
Tehran University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Male
Target Recruitment
18
Inclusion Criteria

Being Diabetic for more than 5 years
male patients
Candidate for pentoxifylline based on endocrinologist diagnosis

Exclusion Criteria

History of diabetic foot ulcer
patient dissatisfaction with enrollment
History of macro or microvascular complications of diabetes (proliferative retinopathy, myocardial infarction, stroke, renal failure requiring dialysis)
Impossibility of dorsal and plantar flexion of the foot
History of any trauma, tumor or other disease in the lower extremities

Study & Design

Study Type
observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Increased perfusion reserve of the lower extremities. Timepoint: Imaging was performed at the beginning of the study (before the intervention) and 4 to 6 weeks after taking the Medication. Method of measurement: Gamma camera imaging.
Secondary Outcome Measures
NameTimeMethod
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