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Study of efficacy of rituximab drug for topical application in oral mucosa in pemphigus vulgaris patients.

Phase 2
Not yet recruiting
Conditions
Health Condition 1: null- ORAL PEMPHIGUS VULGARIS
Registration Number
CTRI/2018/05/014187
Lead Sponsor
Dr SUJAY KHANDPUR
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

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

1. Patients with predominant oral Pemphigus vulgaris (defined as oral involvement with cutaneous involvement less than 1%) or

pure oral mucosal involvement diagnosed on basis of clinical features and ELISA for desmoglein 3 antibody with or without positive tzanck smear and mucosal biopsy

2. Patients in age group of 18-72 years.

3. Patients giving consent for participating in study and obtaining mucosal biopsies.

Exclusion Criteria

1. Patients with pemphigus vulgaris with cutaneous involvement more than 1%.

2. Patients unwilling to give consent for study.

3. Patients with history of significant reaction to intravenous rituximab

4. Patients with severe comorbid illness like patients with malignancy, cardiac failure and uncontrolled diabetes mellitus.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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