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The effect of immunothrapeutic g2 vaccine on treatment of oral lichen planus

Phase 3
Conditions
Oral Lichen Planus.
Other Lichen Planus
L00-L99
Registration Number
IRCT138810112950N1
Lead Sponsor
Dr Mohaghegh Biotechnology Reaserch Center
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
10
Inclusion Criteria

atrophic-erosive oral lichen planus

Exclution criteria:systemic disease-breast feeding and pregnant weman-use of corticosteroids in the last month

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain and burning sensation asking from pateints. Timepoint: Once a week for 12 weeks. Method of measurement: Visual analoge scle-0=no pain and burning and 10 the most pain and burning.;CD4 and CD8 count. Timepoint: before injections-end of injections(13th week). Method of measurement: number of CD4 and CD8 in peripheral blood(by flowcytometry).
Secondary Outcome Measures
NameTimeMethod
Treatment oral lichen planus lesions(reduce size of lesions). Timepoint: Before injection-sixth week-twelveth week. Method of measurement: Ruler(mm2).
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