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The study compares autologous platelet rich fibrin dressings with normal saline dressings in chronic venous leg ulcer patients for ulcer size reduction and quality of life improvement.

Not Applicable
Conditions
Health Condition 1: S801- Contusion of lower leg
Registration Number
CTRI/2024/08/072279
Lead Sponsor
Operation Theater
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1)Chronic venous ulcer of lower extremity having for more than 3 months duration

2)Age more than 18 years

Exclusion Criteria

1)Less than 3 months duration

2)Other causes like arterial/neuropathic/diabetic/vasculitic

3)Patients with Infected ulcers, osteomyelitis affecting the area of the ulcer, ulcers with exposed tendons or bones

4)Patients receiving antiplatelet drugs,anticoagulants,bleeding diathesis.

5)Patients not giving consent for being included in the study

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To measure reduction in ulcer sizeTimepoint: To measure reduction in ulcer size <br/ ><br>1 to 3 months
Secondary Outcome Measures
NameTimeMethod
To measure quality of lifeTimepoint: To measure quality of life <br/ ><br>The Charing Cross Venous Ulcer Questionnaire 23 4 <br/ ><br> <br/ ><br> This questionnaire is composed of 21 items distributed in to 4 domains <br/ ><br>1)Social interaction <br/ ><br>2)Domestic activities <br/ ><br>3)Emotional state <br/ ><br>4)aesthetics <br/ ><br>
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