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comparison between ultrasonic wound debridement and sharp debridement in diabetic foot ulcers

Phase 2
Conditions
diabetic foot ulcer.
personal history of diabetic foot ulcer
Z86.31
Registration Number
IRCT138903271414N21
Lead Sponsor
Endocrine & metabolic research institute-Tehran university of medicak science
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
40
Inclusion Criteria

-patients with known type 1 &2 diabetes
- Diabetic patients with chronic and none healing foot ulcers that need continual debridement
-diabetic patients with diabetic foot ulcer (3 Wagner’s grade without necrosis fashiatis or contiguous joint infection)
-patient's assistance
- ABI=.5-1.2, TOE PRESSURE>50 mmHg
Exclusion criteria:
Diabetic patients with (Wagner’s grade>3 with necrosis fashiatis or contiguous joint infection)
-being metal devices in foot ulcer such as false joint, nail or metal plate, electrical tools

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Rate of healing. Timepoint: 1, 3, 6 months after beginning of debridement or Intervention. Method of measurement: wound area calculation.
Secondary Outcome Measures
NameTimeMethod
Bactericidal effect. Timepoint: Before and after first wound debridement and final wound debridement. Method of measurement: Colony count.;Pain Evaluation. Timepoint: after every wound debridement. Method of measurement: visual analogue scale.
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