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Thymol Dressing in Diabetic foot Ulcer

Phase 1
Recruiting
Conditions
Chronic neuropathic diabetic foot Ulcer.
Type 2 diabetes mellitus with foot ulcer
E11.621
Registration Number
IRCT20170612034485N3
Lead Sponsor
Iranian academic center for education culture and research
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
20
Inclusion Criteria

Chronic neuropathic diabetic foot ulcer (more than 6 weeks) with wound classification Wagner I & II
Full informed consent for recruitment in the study
Age between 18-70 years

Exclusion Criteria

Suspected osteomyelitis
Using corticosteroid or immunosuppressor drug
Chronic renal failure and hemodialysis

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
ocal and systemic side-effects. Timepoint: Every month up to month 6th (or complete healing). Method of measurement: Clinical examination.;Complete wound healing during study (at least 6 months). Timepoint: Every month up to month 6th. Method of measurement: Clinical examination.
Secondary Outcome Measures
NameTimeMethod
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