- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07563400
Plaque Removal in Children Using Charcoal and Nylon Toothbrushes
April 27, 2026 updated by: Mennatullah Yasser Sayed Abou El Enein, Cairo University
Efficacy of Plaque Removal and Antibacterial Properties of Charcoal Infused Bristle Vs Nylon Bristle Toothbrushes in Children: A Randomized Clinical Trial
This study will compare two types of toothbrushes in children: a charcoal-infused bristle toothbrush and a regular nylon bristle toothbrush.
We want to see which toothbrush is better at removing plaque and reducing bacteria in the mouth.
Children will be randomly assigned to use one of the toothbrushes.
We will measure the levels of bacteria in small samples of fluid taken from the gums to see if one toothbrush reduces harmful bacteria more than the other.
Study Overview
Status
Not yet recruiting
Detailed Description
This study is a clinical trial designed to compare the effectiveness of two types of toothbrushes in children aged 6-10.
One group of children will use a toothbrush with charcoal-infused bristles, while the other group will use a standard nylon bristle toothbrush.
All children will be taught the same brushing technique and will brush their teeth twice daily for two minutes using a pea-sized amount of toothpaste.The study will last two weeks.
Researchers will measure four times how much dental plaque is removed from each child's teeth, collect samples from the gums to examine bacteria, and test the toothbrush bristles for bacterial contamination by counting bacterial colonies.The goal is to determine which toothbrush is better at cleaning teeth and reducing harmful bacteria in the mouth.
Study Type
Interventional
Enrollment (Estimated)
50
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Mennatullah Y Abou El Enein
- Phone Number: +201111184215
- Email: mennatullah.yasser@dentistry.cu.edu.eg
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
● Children aged 6 to 10 years.
- Medically free patients with no physical disability.
- Patients must have proper oral hygiene.
- Cooperative patients who will comply with follow-ups.
- Parents who accept to sign informed consent.
Exclusion Criteria:
● Children with a medical condition or physical disability,
- Children undergoing antibiotic treatment
- Children with crowding, fixed or removable orthodontic appliances.
- Children with pre-shedding mobile teeth were excluded from study.
- Children who will be unable to attend follow-up visits.
- Parents refuse to give written formed consent.
- Presence of painful teeth.
- Presence of active carious lesions
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Charcoal-Infused Bristle Toothbrush
Children in this arm will use a soft charcoal-infused bristle toothbrush twice daily for two minutes each time, using a pea-sized amount of fluoride-free toothpaste (Dabur Herb'l, India).
Participants will be trained in the horizontal scrub technique and instructed on proper toothbrush storage to minimize bacterial contamination.
|
manual toothbrush with soft charcoal infused bristles designed fordaily oral hygiene measures.
Participants will be instructed to brush twice daily for two minutes using herbal toothpaste
|
|
Active Comparator: Nylon Bristle Toothbrush
Children in this arm will use a soft nylon bristle toothbrush twice daily for two minutes each time, using a pea-sized amount of fluoride-free toothpaste Participants will be trained in the horizontal scrub technique and instructed on proper toothbrush storage to minimize bacterial contamination.
|
Manual toothbrush with soft nylon bristles designed for daily oral hygiene measures.
Participants will be instructed to brush twice daily for two minutes using herbal toothpaste
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in full-mouth plaque score assessed by O'Leary Plaque Control Index from baseline to 2 weeks
Time Frame: aseline, immediately after training, 1 week, and 2 weeks post-training
|
Full-mouth plaque score will be measured using the O'Leary Plaque Control Index at four time points: baseline (before training), immediately after training, one week, and two weeks post-training.
Each tooth surface (mesial, distal, buccal, and lingual) will be examined.
The plaque score will be expressed as the percentage of plaque-containing surfaces relative to the total number of surfaces examined
|
aseline, immediately after training, 1 week, and 2 weeks post-training
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Estimated)
June 1, 2026
Primary Completion (Estimated)
July 1, 2026
Study Completion (Estimated)
August 1, 2026
Study Registration Dates
First Submitted
April 27, 2026
First Submitted That Met QC Criteria
April 27, 2026
First Posted (Actual)
May 4, 2026
Study Record Updates
Last Update Posted (Actual)
May 4, 2026
Last Update Submitted That Met QC Criteria
April 27, 2026
Last Verified
April 1, 2026
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- CU-PD-RCT-CHARCOAL-2026
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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