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Tissue removal effect of tuttha in any type of ulcer with refferance of hypergranulation of wound

Phase 2
Conditions
Health Condition 1: L768- Other intraoperative and postprocedural complications of skin and subcutaneous tissue
Registration Number
CTRI/2023/02/049500
Lead Sponsor
Dr. Swapnil chavan
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

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

Patient with classical sign & symptom of Hypergranulation and giving voluntary informed consent

Age - 18-70 years

Gender â?? Both

Wound size - 1-5 sq. cm ( using graph paper).

Exclusion Criteria

Patients with uncontrolled diabetes

Patients with infective pathology in hypergranulation.

Immunocompromised patients.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To observe complete resolution of Hypergranulation with tuttha kshar.Timepoint: Schedule once a day <br/ ><br>Duration 7 day <br/ ><br>Follow up 7,15,21 days
Secondary Outcome Measures
NameTimeMethod
To observe complete resolution of Hypergranulation with tuttha kshar.Timepoint: Schedule once a day <br/ ><br>Duration 7 day <br/ ><br>Follow up 7,15,21 days
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