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CHANGES IN NERVE FUNCTION AND DISABILITY IN LEPROSY PATIENTS WHILE ON TREATMENT

Not Applicable
Conditions
Health Condition 1: A309- Leprosy, unspecified
Registration Number
CTRI/2022/02/039908
Lead Sponsor
PGIMER
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

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

1.Patients who give valid consent/assent.

2.Patients of either gender with age 14 and above.

3.All patients being started on anti-leprosy treatment: multidrug therapy (MDT) or alternative therapy in cases with drug resistanceas per WHO guidelines69

Exclusion Criteria

1.Patients who are not willing to provide consent for the study.

2.Patient of age <14 years

3.Patients at risk of a neuropathy other than leprosy, i.e. diabetes, alcoholism, risk group for HIV infection, patients with a family history of hereditary neuropathy.

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To assess nerve function impairment(NFI) and disability status in leprosy patients on anti-leprosy treatment(ALT)Timepoint: Will be done as 3 monthly assessment till 1 year study period
Secondary Outcome Measures
NameTimeMethod
To study the predictors of changes (improvement or worsening) in nerve function impairment(NFI)Timepoint: 1 year
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