oral malodor. halitosis
Conditions
Interventions
Intervention 1: using from green tea mouth wash for one week two times a day in intervention group. Intervention 2: using placebo mouth wash for one week two times a day in control group.
Treatment - Drugs
using from green tea mouth wash for one week two times a day in intervention group
using placebo mouth wash for one week two times a day in control group
Sponsors
Vice Chanceller of Isfahan University of Medical Sciences
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Inclusion criteria: Patients who complain of oral malodor; Patients who their halitosis will be confirmed after clinical examination. Exclusion criteria: Patients who were not willing to participate in the study; female patients in their period of menstruation; smoking people; those with systemic diseases.
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Oral halitosis with organoleptic method. Timepoint: before intervention, one weak after intervention. Method of measurement: Fundamentals of Organoleptic method: The patient will be asked to keep his/her mouth closed for two minutes and then exhale out the air. To determine the severity of the oral malodor, the researcher will measure the severity of the patient’s halitosis from the distance of 10 cm. and 50 cm., and then the severity of patient’s halitosis is classified as following five categories based on the organoleptic method: 0 = no smell of halitosis, 1= low, 2= moderate, 3= severe, 4 = very intense smell. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactParichehr Behfarnia
Isfahan University of Medical Science
Outcome results
None listed