The Preventive Effect of 2-years Use of Hydroxyapatite Containing Toothpastes in Children.

Sponsor
Università degli Studi di Sassari (Other)
Overall Status
Completed
CT.gov ID
NCT04906291
Collaborator
(none)
610
1
4
33
18.5

Study Details

Study Description

Brief Summary

The aim of this RCT was to verify the caries preventive efficacy of toothpastes containing biomimetic hydroxyapatite (H.A.) complex in children compared to traditional fluoridated toothpastes. In total 610 children of two age groups (4-5 years and 6-7 years at baseline) were enrolled. Four toothpastes, two containing fluoride-substituted hydroxyapatite (H.A.F.) (1000 and 1450 ppm F-) and magnesium-, strontium-, carbonate-substituted hydroxyapatite, in a chitosan matrix and two traditional fluoridated toothpastes (1000 and 1450 ppm F-) without other active components were administered randomly to two groups with younger children (Gyoung) and to two groups with older children those containing1450 ppm F (GOLD) during 24 months. A standardized questionnaire was administered to parents/caregivers to gain information regarding caries risk factors. Caries evaluation was performed at school using ICDAS, scoring lesions as initial (up to score 2), moderate (scores 3-4) and severe (scores 5-6).

Condition or Disease Intervention/Treatment Phase
  • Other: Toothpaste use
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
610 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Triple (Participant, Investigator, Outcomes Assessor)
Primary Purpose:
Prevention
Official Title:
The Caries Preventive Effect of 2-years Use of Hydroxyapatite Containing Toothpastes in Children. A Triple-blind Randomized Placebo-controlled Clinical Trial.
Actual Study Start Date :
Feb 1, 2018
Actual Primary Completion Date :
Jun 30, 2020
Actual Study Completion Date :
Oct 31, 2020

Arms and Interventions

Arm Intervention/Treatment
Experimental: H.A.F. toothpaste (1000 ppm F-)

The children were instructed to brush their teeth for at least two minutes after each main meal (three times/day).

Other: Toothpaste use
Brushing three times a day

Active Comparator: Fluoridated toothpaste (1000 ppm F-)

The subjects were instructed to brush their teeth for at least two minutes after each main meal (three times/day).

Other: Toothpaste use
Brushing three times a day

Experimental: H.A.F. toothpaste (1450 ppm F-)

The subjects were instructed to brush their teeth for at least two minutes after each main meal (three times/day).

Other: Toothpaste use
Brushing three times a day

Active Comparator: Fluoridated toothpaste (1450 ppm F-)

The subjects were instructed to brush their teeth for at least two minutes after each main meal (three times/day).

Other: Toothpaste use
Brushing three times a day

Outcome Measures

Primary Outcome Measures

  1. Caries Progression rate [2 year]

    . Caries incidence rate was calculated on each tooth (primary and permanent) as the unit of analysis

Eligibility Criteria

Criteria

Ages Eligible for Study:
4 Years to 8 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Written declaration of informed consent signed by parents/guardians;

  • Age between 4-5 years and 6-7 years; Good general health, as assessed by the examiners;

  • Agreement of not to use any oral hygiene products except for the toothpastes provided for the duration of the study.

Exclusion Criteria:
  • Ongoing oral or dental treatment except for emergency treatment;

  • Known allergic reaction to an oral hygiene product and/or medication and/or dental material previously used in the mouth or pharynx;

  • Allergy to one of the components of the test products or the standard toothpaste;

  • Participation in another clinical trial either currently or within the last 30 days;

  • Antibiotic therapy within the past 3 months.

Contacts and Locations

Locations

Site City State Country Postal Code
1 University of Sassari, Dept of Surgery, Microsurtgery and Medicine Sciences Sassari SS Italy 07100

Sponsors and Collaborators

  • Università degli Studi di Sassari

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Guglielmo Campus, Associate Professor in Preventive Dentistry, Università degli Studi di Sassari
ClinicalTrials.gov Identifier:
NCT04906291
Other Study ID Numbers:
  • USassari02.2017
First Posted:
May 28, 2021
Last Update Posted:
May 28, 2021
Last Verified:
May 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Guglielmo Campus, Associate Professor in Preventive Dentistry, Università degli Studi di Sassari

Study Results

No Results Posted as of May 28, 2021