A comparative assessment of Salvia officinalis gel and Triamcinolon asetonolyd gel regarding the duration and symptoms of oral lichenoid reactio
Phase 4
- Conditions
- lichenoid reaction.Lichen simplex chronicus
- Registration Number
- IRCT2015061422706N1
- Lead Sponsor
- Isfahan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 60
Inclusion Criteria
maximum age of 60 years; minimum age of 20 years; non-pregnant; non-breastfeeding women; ability to remain during the study period. exclusion criteria:The patients with allergy to plant products; drug abuse; those who were reluctant to cooperate.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Extent of lesions. Timepoint: baseline, seventh day, the fourteenth day. Method of measurement: 0 to 5according to the parameters mentioned by Buajeeb.;Pain. Timepoint: baseline, seventh day, the fourteenth day. Method of measurement: according to the Visual Analog Scale (VAS) from 0 to 10.;Drug type. Timepoint: baseline, seventh day, the fourteenth day. Method of measurement: method.
- Secondary Outcome Measures
Name Time Method Burning and sensivity from drug. Timepoint: baseline, seventh day, the fourteenth day. Method of measurement: ask the patient.