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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03053882
Other study ID # SBMU
Secondary ID
Status Completed
Phase N/A
First received February 4, 2017
Last updated February 12, 2017
Start date January 2015
Est. completion date June 2016

Study information

Verified date February 2017
Source Shahid Beheshti University of Medical Sciences
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Background:

Herbal remedies can have the role of prevention and control of bad breath Since in the previous studies, therapeutic and antibacterial effect of green tea and peppermint had been proven .we studied and compared the effects of green tea and peppermint mouthwashes on halitosis.

Materials and Methods:

This single-blind clinical trial study with cross over design total of 88 volunteer dental students who complained bad breath and had organoleptic score (>= 2) and higher average test scores were enrolled. The students were divided randomly into two groups Green Tea - Peppermint were assigned. Organoleptic test in the baseline, on the 7 day, 14 and 21 measured after rinsing the mouthwashes .As well as the satisfaction of both plants on the last day was considered. Data analysis was performed using tests; Wilcoxon signed rank test, Mann Whithney u, GEE (Generalized Estimating Equation -ordinal logistic regression).


Recruitment information / eligibility

Status Completed
Enrollment 88
Est. completion date June 2016
Est. primary completion date January 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 30 Years
Eligibility Inclusion Criteria:

organoleptic number equal to or higher 2 no foods (garlic and onion) 48 hours before organoleptic test

Exclusion Criteria:

systemic disease

- use of antibiotics during study use of other mouthwash during study

Study Design


Related Conditions & MeSH terms


Intervention

Other:
mouthwash
mouthwash containing herbal peppermint or green tea

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Shahid Beheshti University of Medical Sciences

Outcome

Type Measure Description Time frame Safety issue
Primary evaluation of changes in organoleptic score 0-5 organoleptic scale baseline,7 days,14 days,21 days
Secondary satisfaction of patients questionnaire 21 days
See also
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