A clinical and Investigative study of Lichen Planus pigmetosus

Not Applicable

Completed

• Conditions: Health Condition 1: null- Lichen planus pigmentosus

• Registration Number: CTRI/2013/03/003491
• Lead Sponsor: Indian Association of Dermatologists Venereologists and Leprologists

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 24 November 2021

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 30

Inclusion Criteria

1.Patients willing to voluntarily participate in the study with a written informed consent.

2.Age group of above 18 years.

3.Untreated cases of LPP willing for necessary investigations

Exclusion Criteria

1.Patient not willing to give consent.

2.Immunocompromised patients and pregnant women.

3.Patients who have taken treatment for LPP in the last 3 months.

Study & Design

• Study Type: Observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Epidemiological, Clinical and Histopathological and immunohistochemical data in Lichen planus pigmentosus.Timepoint: one year

Secondary Outcome Measures

Name	Time	Method
ilTimepoint: nil