Skip to main content
OpenTrials
Completed

NCT Number: NCT05560945

2-year Caries Clinical Study: Arginine Fluoride-Free Toothpastes vs. NaF Toothpaste

The objective of this study is to evaluate the anticaries efficacy for three dentifrices (1.5% arginine in a calcium base, 8.0% arginine in a calcium base, and 0.32% sodium fluoride in a silica base) in a two-year caries clinical study

Completed

Looking for future studies?

Notify Me

Key information

Age range

10 year–14 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

School of Stomatology, Xian Jiaotong University, Xi'an, Shaanxi, China

Loading trial locations.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Informed Consent Form signed by parent or legal guardian to permit participation of their child in the study
  • Willingness and ability to use the assigned products according to instructions, availability for all appointments and likelihood of completing the clinical trial.
  • Children ages 10-14 years at baseline.
  • Presence of second molars or evidence of erupting permanent molars.
  • Subjects should be of good general health as evidenced by a review of the medical history.
  • Presence of two or more active caries lesions (ICDAS scores of 2 or greater) and with a previous caries experience (DMFS ≥ 2). Exclusion Characteristics
  • Subjects presenting with any of the criteria below will be excluded from the study:
  • Presence of fixed or removable prosthetic appliance or orthodontic treatment involving more than four permanent teeth.
  • Use of medication that could increase the risk of developing dental caries, i.e. medication that reduces saliva flow.
  • Long-term antibiotic therapy.
  • Children with cognitive and/or motor impairment.
  • Severe malocclusion.
  • Presence of severe caries (ICDAS 5 or 6) on five or more teeth.
  • Evidence of moderate to severe periodontal disease.
  • Participation in any other clinical study within the 30 days preceding the clinical study.
  • History of allergies or other adverse reactions to arginine, or oral care products, or their ingredients.
  • Pregnant or lactating.

Treatment and study plan

0.32% Sodium Fluoride Dentifrice Toothpaste

Drug

Toothpaste

1.5% Arginine Dentifrice

Drug

Toothpaste

8.0% Arginine Dentifrice

Drug

Toothpaste

Primary outcomes

  1. The primary efficacy endpoint will be the incremental subject-wise Decayed Missing Filled Surfaces score after 2 year product use.

    Time frame: 2 year

    the minimum score is 0, maximum score is 4/5 depending on the tooth number and a higher score represents a worse outcome

  2. The primary efficacy endpoint will be the incremental subject-wise Decayed Missing Filled Teeth scores after two year of product use.

    Time frame: 2 year

    the minimum score is 0, maximum score is 4/5 depending on the tooth number and a higher score represents a worse outcome

Sponsors and collaborators

Lead sponsor

Colgate Palmolive

Industry

Registry information

Official study title

Clinical Investigation Examining the Anticaries Efficacy of Three Dentifrices (1.5% Arginine in a Calcium Base, 8.0% Arginine in a Calcium Base, and 0.32% Sodium Fluoride in a Silica Base): a Two-year Caries Clinical Study

Important dates

Study start
2019
Primary completion
2022
Study completion
2022
First posted
Sep 30, 2022
Registry last updated
Oct 3, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.