Preparation of mouthrinse from extract of aerial parts of zataria multiflora &frankincense as well as evaluation of their clinical effects on oral and dental diseases.
Not Applicable
- Conditions
- Oral& teeth health indexes..Certain infectious and parasitic diseases
- Registration Number
- IRCT2017072435263N1
- Lead Sponsor
- vice chncellor for research of tabriz university of medical sciences.
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 140
Inclusion Criteria
Enclusion criteria: 1-plaq index above 1.9. 2-gingival index above 1. 3- not receiving any antibiotic or anti inflamatory drug in the long of this study and one month ago. 4- being literate. 5-having a call number. 6-the desire to participate in this study. Exclusion criteria: 1-systemic diseases. 2-using drugs that cause inflammation in the gum or excerbate the gum diseases. 3-smoking . 4-use of other mouthrinses from four weeks ago . 5-sensitization to plant materials . 6-methabolic diseases(diabet,hyperthyroidism,etc). 7-pregnancy. 8-Doing any dental practices outside the scope of the study. 9-orthodontic patients.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Bleeding index. Timepoint: Before intervention ,fourteen and twenty one day after intervention. Method of measurement: Salcos test and giving grade between 0-3 for it.;Teeth color index. Timepoint: Before intervention and fourteen and twenty one day after intervention. Method of measurement: Abservation and giving a grade between 0-3 for it.;Gingivit index. Timepoint: Before intervention and fourteen and twenty one day after intevention. Method of measurement: Abservation and giving grade between 0-3 for it.;Plaque index. Timepoint: Efore intervention and fourteen and twenty one day after intevention. Method of measurement: Chewing plaque search tablet and counting the number of plaques.
- Secondary Outcome Measures
Name Time Method Possible advers effects. Timepoint: Twenty one day after interaction. Method of measurement: Questionnaire.