Role of 1 percent topical Spirulina gel as intervention in participants having Oral Lichen Planus
Phase 4
- Conditions
- Health Condition 1: K121- Other forms of stomatitis
- Registration Number
- CTRI/2024/06/069548
- Lead Sponsor
- Dr Nitika Aggarwal
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1) All clinically Diagnosed cases with atrophic, erosive, reticular or any other form
of oral lichen Planus.
2) Patients above 21 years of age.
3) Patients with no contraindications or documented allergies to the
medications which are being used for study.
4) Patients willing to participate in the study.
Exclusion Criteria
1) Previously treated patients of oral lichen planus in last 3 months or those
who have left treatment in-between, or undergoing any other
treatment modality.
2) Patients with co-existing systemic illness like diabetes mellitus, hypertension.
3) Pregnant and lactating mother.
Study & Design
- Study Type
- PMS
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Burning sensation <br/ ><br>(Visual analog <br/ ><br>scale), <br/ ><br>Size of the lesion <br/ ><br>(using vernier <br/ ><br>caliper), <br/ ><br>Clinical assessment <br/ ><br>(Thongprasom <br/ ><br>score)Timepoint: weekly for 4 weeks, after that 15 days for 1 month
- Secondary Outcome Measures
Name Time Method To record the adverse reactions, if any, with both the drugs in either of the two groups, <br/ ><br>To record the recurrence of the lesion in any of the two groupsTimepoint: weekly for 4 weeks, after that 15 days for 1 month