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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04779502
Other study ID # 131619
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 12, 2020
Est. completion date November 17, 2020

Study information

Verified date March 2021
Source University of Baghdad
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

the efficacy of commercially available oregano essential oil mouthwash in the reduction of oral halitosis was compared to chlorhexidine and distilled water and the results showed significant reduction of organoleptic tongue and floss scores and BANA test scores compared to placebo


Description:

the results showed that oregawash showed a comparable effect to chx in reducing oral halitosis


Recruitment information / eligibility

Status Completed
Enrollment 54
Est. completion date November 17, 2020
Est. primary completion date November 15, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 23 Years
Eligibility Inclusion Criteria: 1. Organoleptic score was >2 at baseline. 2. Participants between 18-23 years of age. 3. The subjects had no systemic disease and were not taking antibiotics or receiving other antimicrobial therapy. 4. The subjects did not receive the same time treatment for their halitosis. Exclusion Criteria: 1. Smokers, alcoholics and drug addicts. 2. Patients with periodontitis or pocket depth >6 mm. 3. Patients taking drugs which induced xerostomia. 4. Subjects consuming spicy food: garlic or onions two days before examination. 5. Patients with orthodontic appliances or removable dentures. 6. pregnancy

Study Design


Related Conditions & MeSH terms


Intervention

Other:
oregawash
mouthwash containing oregano essential oil
corsodyl
0.2% chlorhexidine mouthwash
placebo
distilled water

Locations

Country Name City State
Iraq Univeristy of Baghdad Baghdad Rasafa

Sponsors (1)

Lead Sponsor Collaborator
MOHAMED SAEED M. ALI

Country where clinical trial is conducted

Iraq, 

Outcome

Type Measure Description Time frame Safety issue
Primary organoleptic tongue and floss scores organoleptic measuements 9 month
Secondary BANA test chair side BANA test 9 month
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