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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.

Preparation of mouthrinse from extract of aerial part of zataria multiflora &frankincense as well as evaluation of their clinical effects on oral and dental healthcare's indexes.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2017072435263N1
Enrollment
140
Registered
2017-08-31
Start date
2017-08-30
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Oral& teeth health indexes.. Certain infectious and parasitic diseases

Interventions

Intervention 1: Using herbal mouthrinse contain zataria multiflora extract for 21day (twice in a day)as one of the intervention groupes. Intervention 2: Using mouthrinse contain chlorhexidine for 21d
Treatment - Drugs
Using herbal mouthrinse contain zataria multiflora extract for 21day (twice in a day)as one of the intervention groupes.
Using mouthrinse contain chlorhexidine for 21day (twice in a day)as control group
Using herbal mouthrinse contain both of zataria multiflora &frankincense extract for 21 day (twice In day) as one of the intervention group
Using herbal mouthrinse contain frankincense extract for 21day (twice in a day) as one of the intervention group.

Sponsors

vice chncellor for research of tabriz university of medical sciences.
Lead Sponsor

Eligibility

Sex/Gender
All
Age
15 Years to 55 Years

Inclusion criteria

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

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
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

MeasureTime frame
Possible advers effects. Timepoint: Twenty one day after interaction. Method of measurement: Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactZoleikha khoshbakht

Tabriz university of medical sciences

Khoshbakhtz@tbzmed.ac.ir+98 44 3348 7232

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026