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A clinical study to compare the dental plaque removal of an electric versus a manual toothbrush with children age 3-6 years and 7-9 years.

Not Applicable
Completed
Conditions
General healthy children between 3-9 years old with evidence of afternoon dental plaque
Oral Health
Registration Number
ISRCTN10901742
Lead Sponsor
Procter & Gamble (United States)
Brief Summary

2020 results in https://pubmed.ncbi.nlm.nih.gov/33225464/ (added 08/06/2021)

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
All
Target Recruitment
41
Inclusion Criteria

1. Come to the site with a parent or legal guardian which has given written informed consent and received a copy of their consent following the guidelines of the Institutional Review Board of Hadassah University
2. Be 3 to 9 years old
3. Be in good general health condition as determined by the Investigator/designee based on a review/update of their medical history for participation in the study
4. Possess a minimum of 16 natural teeth with facial and lingual scorable surfaces
5. Agree to delay any elective dentistry, including dental prophylaxis and to report any non-study dentistry received for the duration of this study
6. Have evidence of afternoon dental plaque (per investigator’s discretion)
7. Agree to maintain their same regular at-home oral hygiene routine and oral care products for this study duration
8. Agree not to participate in any other oral care study for the duration of this study
9. Agree to return for their scheduled visits and to follow all study procedures
10. Refrain from eating, drinking* and chewing gum for at least 3 hours prior to this visit and agree to follow the same restriction prior to all visits; *(Exception being allowed small sips of water up until 45 minutes prior to their appointment time.)
11. Refrain from performing any other oral hygiene after their regular morning oral hygiene prior to this visit and agree to the same restriction prior to all visits

Exclusion Criteria

1. Any disease or condition that could be expected to interfere with examination procedures or with the subject safely completing this study (including allergies to dyes or the need for pre-medication prior to dental procedures)
2. Any condition requiring immediate dental treatment
3. Fixed facial or lingual orthodontic appliances
4. Use of antibiotics within two weeks prior to study initiation
5. Receive dental prophylaxis within one month prior to study initiation

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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