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comparison of Injectable platelet rich fibrin and steroids in oral lichen planus

Phase 3
Conditions
Health Condition 1: D899- Disorder involving the immune mechanism, unspecifiedHealth Condition 2: K137- Other and unspecified lesions of oral mucosa
Registration Number
CTRI/2023/11/060372
Lead Sponsor
PGIDS Rohtak
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

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

1)Clinically symptomatic and histologically proven cases of oral lichen planus in accordance to WHO criteria.

2)Patient who give written consent to participate in the study

Exclusion Criteria

)Patient under the age of 18 years.

2)Histopathological signs of moderate to severe dysplasia.

3)Patients with genital or cutaneous involvement.

4)History of topical or systemic corticosteroids therapy within one month prior to recruitment.

5)Allergic or contraindication to administration of injectable corticosteroids.

6)Patients with Hb levels <9 gm/dl and platelet count < 1 lakh/dl.

7)Patients with known hematological disease, chronic liver disease and psychiatric disorders.

8)Smokers or chewable tobacco users.

9)Patients with pregnancy or lactating mothers.

Study & Design

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