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Effect of pentoxifylline topical ointment on wound healing

Phase 3
Recruiting
Conditions
Bedsore.
Registration Number
IRCT20150721023282N18
Lead Sponsor
Esfahan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
44
Inclusion Criteria

Infection of stage 2 or 3 bedsores in one or more areas

Exclusion Criteria

Smoking now
Use of immunosuppressive drugs in the last 3 months
Having a coagulation disorder (such as hemophilia)
Use of medications or supplements effective in wound healing (phenytoin, glucocorticoids, anticancer drugs and products containing vitamin C, vitamin A or Zinc) in the last 3 months

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Percent of Decrease in Ulcer Size. Timepoint: Baseline, 7 and 14 Days after Initiation of Intervention. Method of measurement: Ruler.
Secondary Outcome Measures
NameTimeMethod
The Number of Cases with Peri-Ulcer Erythema. Timepoint: Baseline, 7 and 14 Days after Initiation of Intervention. Method of measurement: Observation.
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