Health Condition 1: L438- Other lichen planus
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Clinically diagnosed Oral Lichen Planus patients willing to participate in the trial with no history of prior treatment for the same
Exclusion criteria
Exclusion criteria: 1. Patients with known history of hypersensitivity to Triamcinolone Acetonide and Ashwagandha 2. Patients diagnosed with other intra oral lesions 3. Pregnant women and lactating mothers 4. Immunocompromised patients
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Intensity of burning sensation will be assessed using a Visual Analogue Scale (VAS)Timepoint: Baseline, 30 Days, 60 Days, 90 Days | — |
Secondary
| Measure | Time frame |
|---|---|
| Size of the lesion will be measured in square centimeters (cm2) using divider and scaleTimepoint: Baseline, 30 Days, 60 Days, 90 Days | — |
Countries
India
Contacts
Swargiya Dadasaheb Kalmegh Smruti Dental College and Hospital Hingna