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Evaluation of advanced dressing procedure in comparison with the standard dressing procedure for Healing long-term Wounds

Not Applicable
Conditions
Health Condition 1: 8- Other Procedures
Registration Number
CTRI/2024/07/071302
Lead Sponsor
Dr Ranganath V S
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

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

Participants with chronic wound for more than six weeks and have failed to heal by conventional treatments.

Wound size of less than 20cm2.

Both male and female participants.

Age 20 years or older.

Have a normal platelet count in range of 1,50,000- 4,50,000 cells/mm3.

Have a normal PT time: 11- 16 seconds.

Ability to provide informed consent or have a legally authorized representative able to provide consent on behalf of the participant.

Willingness to comply with study procedures and follow-up visits.

Adequate understanding of the study requirements and ability to communicate with study personnel.

Exclusion Criteria

Presence of an active infection at the ulcer site.

Patients on anticoagulants (warfarin, heparin).

Pregnant and lactating women.

Patients suffering from leukaemia, septicaemia, impaired platelet function or other haematological disorders.

Patients with hypoproteinaemia.

Patients taking long term steroid containing drugs or using steroid ointments on wounds.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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