CTRI/2023/11/060372Not yet recruitingPhase 3
Comparative efficacy of injectable platelet rich fibrin and triamcinolone acetonide in symptomatic oral lichen planus
PGIDS Rohtak0 sites0 target enrollmentStarted: TBDLast updated:
Trial Snapshot
- Phase
- Phase 3
- Status
- Not yet recruiting
- Sponsor
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
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.
Investigators
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