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tility of CB-NAAT (a diagnostic test) in diagnosing cases of skin tuberculosis.

Not Applicable
Completed
Conditions
Health Condition 1: L088- Other specified local infections of the skin and subcutaneous tissue
Registration Number
CTRI/2019/02/017549
Lead Sponsor
King Georges Medical University
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
44
Inclusion Criteria

(a) Patients clinically diagnosed as cutaneous TB and who give consent to participate in

the study

Exclusion Criteria

(a) Who have taken ATT in last one year

(b) Contra-indication for biopsy or FNAC like bleeding and clotting disorders

(c) Patients with severe debilitating and chronic illness like Hepatitis B,C, malignancy,

uncontrolled diabetes etc

(d) Not willing to participate in study

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To assess and compare the efficacy of CBNAAT, culture and histopathological <br/ ><br>examination (including staining for AFB) in diagnosing cases of cutaneous TB.Timepoint: 1.5 years
Secondary Outcome Measures
NameTimeMethod
Assessment and comparison of Rifampicin resistance results shown <br/ ><br>by CBNAAT and DST (for cases that show culture growth).Timepoint: 1.5 years
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