CTRI/2023/08/056156
Not yet recruiting
未知
Evaluation of efficacy of topical 0.1% Triamcinolone acetonide and topical 0.1% Tacrolimus in the management of symptomatic Oral Lichen Planus followed by In silico analysis- A randomized observer blinded clinical study. - NI
Overview
- Phase
- 未知
- Status
- Not yet recruiting
Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
Inclusion Criteria
- •Clinico\- histopathologically diagnosed cases of Oral Lichen
- •1\. Patients with symptoms of pain and burning sensation
- •secondary to Oral Lichen Planus.
- •2\. Patients willing to participate in the study
Exclusion Criteria
- •Topical or systemic medication for treatment of Oral Lichen Planus up to 4 weeks prior to the study
- •Histopathological examination with atypical or lichenoid
- •dysplastic features.
- •1\. Patients with asymptomatic oral lesions.
- •2\. Patients with other mucosal diseases.
- •3\. Patients with history of any allergy.
Investigators
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