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NCT04830176 Clinical Trial

Role of Herbal Dentifrices in the Management of Plaque Induced Gingivitis

Plaque, Dental Clinical Trial

Official title:
Role of Moringa Dentifirice in the Management of Plaque Induced Gingivitis. A Clinical Crossover Study

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT04830176
Other study ID # D-F-19-03-04
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 20, 2021
Est. completion date March 28, 2021

Study information
Verified date April 2021
Source Ajman University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The clinical cross over study involves the use of two herbal based dentifirices moringa and miswak and its efficacy in reducing plaque induced gingivitis. The patients selected are provided with details regarding the research format and consent taken.

Description:

The clinical cross over study involves use of miswak and moringa dentifrices. The patients selected are 30 in no and are selected based on having gingival inflammation due to plaque accumulation. All other cases related to gingival inflammation along with patients with underlying systemic disease are excluded from the study. At baseline, plaque and gingival scores are recorded, followed by giving one of the dentifrice to the patient for brushing. The patients are asked to brush twice a day and asked to report after 72 hrs, following which another recording of plaque and gingival scores are recorded. The patients are then asked to use their own tooth paste for a period of 2 weeks as a wash out period and recalled after this 2 week interval. The patients are then given the second dentifrice and asked to brush for 72 hrs and then asked to report again for a plaque and gingival score evaluation.

Recruitment information / eligibility
Status Completed
Enrollment 30
Est. completion date March 28, 2021
Est. primary completion date March 20, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 20 Years to 60 Years
Eligibility Inclusion Criteria: - subjects having only plaque induced gingival inflammation Exclusion Criteria: - Subjects having gingival inflammation related to underling systemic diseases - Subjects taking medications - Gingival inflammation related to other causes

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• dentifrice
use of dentifrices for brushing

Locations
Country Name City State
India AB shetty Institute of dental sciences Mangaluru

Sponsors (2)
Lead Sponsor Collaborator
Ajman University A B Shetty Memorial Institute of Dental Science

Country where clinical trial is conducted

India, 

Outcome
Type Measure Description Time frame Safety issue
Primary plaque scores plaque score recorded using calibrated periodontal probes 72 hours
Secondary Gingival inflammation scores Gingival bleeding scores recorded using caliberated periodontal probes 72 hours
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