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se of Homoeopathic Medicine in thetreatment of Lichen Planus

Phase 2
Conditions
Health Condition 1: L439- Lichen planus, unspecified
Registration Number
CTRI/2024/05/066823
Lead Sponsor
ational Institute of Homoeopathy
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

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

Subjects must be able to understand and comply with the requirements of the study and

communicate with the investigator

Subjects must give written, signed, and dated informed consent before any study related

activity is performed

Patients of age group 12 to 60 years

Patients of all sexes and of all religions and of different socioeconomic status

Subjects must have clinical features of LP

Exclusion Criteria

Individuals with skin conditions that might confound the diagnosis or evaluation of lichen

planus

pregnant or breastfeeding individuals

Critically ill patient, immunecompromised patient

Patient suffering from any other systemic diseases

Diagnosed cases of unstable mental or psychiatric illness

Patient or Parents of patient unwilling to give consent

Patient having any substance abuse

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
changes in Lichen Planus Severity Index ScoreTimepoint: changes in Lichen Planus Severity Index Score At baseline and 6 months
Secondary Outcome Measures
NameTimeMethod
Comparing previous photographs of lesionsTimepoint: 0 and 6 months
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