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Role of Herbal Dentifrices in the Management of Plaque Induced Gingivitis

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04830176
Enrollment
30
Registered
2021-04-05
Start date
2021-01-20
Completion date
2021-03-28
Last updated
2021-04-08

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

Conditions

Gingiva; Infection, Plaque, Dental

Keywords

miswak, moringa, plaque, gingival bleeding

Brief 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.

Detailed 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.

Interventions

use of dentifrices for brushing

Sponsors

A B Shetty Memorial Institute of Dental Science
CollaboratorOTHER
Ajman University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
PREVENTION
Masking
DOUBLE (Subject, Caregiver)

Masking description

Both the participant and the care provider were masked. They were unaware of the paste they were using as it was marked alphanumerically

Intervention model description

sample size of 30- First group of 15 subjects recording of plaque and gingival scores were recorded. Patients were given first dentifrice and asked to brush for 72 hours and then asked to report. A washout period of 2 weeks followed. The next round, the subjects were given the second dentifrice and asked to brush for 72 hrs and then after a period of 3days asked to report

Eligibility

Sex/Gender
ALL
Age
20 Years to 60 Years
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frameDescription
plaque scores72 hoursplaque score recorded using calibrated periodontal probes

Secondary

MeasureTime frameDescription
Gingival inflammation scores72 hoursGingival bleeding scores recorded using caliberated periodontal probes

Countries

India

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026