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Fluoride vs Probiotic Toothpaste for Caries Prevention

Study on Influencing Factors of Dental Caries in 4- to 5-Year-Old Children in Pingdu City and the Effectiveness of Different Toothpastes in Preventing Childhood Caries

This clinical trial had two objectives. The first was to compare the effectiveness of 950 ppm fluoride toothpaste versus probiotic toothpaste in preventing dental caries in 4- to 5-year-old children. The second was to understand how children's oral hygiene habits and dietary habits influence the development of dental caries.

The main questions it aimed to answer are:

  • Does fluoride toothpaste reduce new caries more than control toothpaste?
  • Does probiotic toothpaste reduce new caries more than control toothpaste?
  • Which oral hygiene and dietary habits are risk factors for dental caries?

Researchers compared fluoride toothpaste and probiotic toothpaste to a control toothpaste (without active ingredients).

Participants were asked to complete the following tasks:

  • Complete a questionnaire about their oral hygiene and dietary habits at baseline
  • Undergo oral health examinations at baseline and after 12 months
  • Brush their teeth twice daily (morning and before bedtime) with their assigned toothpaste for 12 months
  • Use a pea-sized amount of toothpaste each time
  • Brush under the supervision of parents to ensure brushing quality

Studieöversikt

Detaljerad beskrivning

Study design and setting This was a cross-sectional survey combined with a prospective, randomized, single-blind, controlled trial conducted in Pingdu City, China. Five kindergartens (two urban, three rural) were randomly selected.

Cross-sectional survey phase A total of 540 children aged 4-5 years underwent oral examinations performed by two trained and calibrated dentists. Parents completed a questionnaire on children's oral hygiene behaviors and dietary habits.

Randomized controlled trial phase

After baseline assessment, 508 children were randomly assigned to three groups (1:1:1):

  • Fluoride toothpaste group: 950 ppm fluoride toothpaste
  • Probiotic toothpaste group: Toothpaste containing Lactobacillus paracasei
  • Control group: Toothpaste without active ingredients

Participants brushed twice daily (morning and before bedtime) with a pea-sized amount of assigned toothpaste for 12 months under parental supervision. Kindergarten teachers supervised lunchtime brushing. All participants received standardized oral health education at baseline and each semester.

Compliance monitoring Compliance was assessed using daily toothbrushing record cards and collected toothpaste tubes. Only children with moderate or good compliance were included in final analysis.

Ethical approval The study was approved by the Human Research Ethics Committee of The Affiliated Hospital of Qingdao University (Approval No.: QYFYWZLL29924). Written informed consent was obtained from parents or legal guardians, and verbal assent from each child.

Studietyp

Interventionell

Inskrivning (Faktisk)

508

Fas

  • Fas 4

Kontakter och platser

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Studieorter

    • Shandong
      • Qingdao, Shandong, Kina, 266003
        • The Affiliated Hospital of Qingdao University

Deltagandekriterier

Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.

Urvalskriterier

Åldrar som är berättigade till studier

  • Barn
  • Vuxen

Tar emot friska volontärer

Ja

Beskrivning

Inclusion Criteria:

  • Age 4-5 years (48-59 months)
  • Informed consent obtained from parents or guardians, with permanent residence in Pingdu City and willingness to actively cooperate throughout the study
  • No long-term medication use
  • Absence of systemic diseases and mental health disorders

Exclusion Criteria:

  • Not meeting any of the inclusion criteria
  • Children whose parents or guardians did not provide informed consent
  • Presence of systemic diseases or mental health disorders
  • Long-term medication use

Studieplan

Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.

Hur är studien utformad?

Designdetaljer

  • Primärt syfte: Förebyggande
  • Tilldelning: Randomiserad
  • Interventionsmodell: Parallellt uppdrag
  • Maskning: Enda

Vapen och interventioner

Deltagargrupp / Arm
Intervention / Behandling
Experimentell: 950 ppm Fluoride Toothpaste
Children brushed their teeth three times daily (after breakfast, after lunch, and before bedtime) using 950 ppm fluoride toothpaste (comeno Fluoride Toothpaste, 3M, USA). A pea-sized amount (approximately 0.5 g) was used each time. The intervention lasted 12 months.
Contains 950 ppm fluoride. Used for tooth brushing three times daily.
Andra namn:
  • comeno fluoride toothpaste
Experimentell: Probiotic Toothpaste
Children brushed their teeth three times daily (after breakfast, after lunch, and before bedtime) using probiotic toothpaste containing Lactobacillus paracasei (Yunnan Baiyao Children's Toothpaste, Yunnan Baiyao, China). A pea-sized amount (approximately 0.5 g) was used each time. The intervention lasted 12 months.
Contains Lactobacillus paracasei. Used for tooth brushing three times daily.
Andra namn:
  • Lactobacillus paracasei
  • Yunnan Baiyao Children's Toothpaste
Aktiv komparator: Control Toothpaste
Children brushed their teeth three times daily (after breakfast, after lunch, and before bedtime) using control toothpaste without active ingredients (Beilele Children's Toothpaste, Lengsuanling, China). A pea-sized amount (approximately 0.5 g) was used each time. The intervention lasted 12 months.
Toothpaste without active fluoride or probiotic ingredients. Used for tooth brushing three times daily.
Andra namn:
  • Beilele Children's Toothpaste

Vad mäter studien?

Primära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Number of newly severe decayed surfaces
Tidsram: Baseline to 12 months
The change in the number of severe decayed surfaces (ICDAS codes 5-6, indicating caries approaching or exposing the pulp) per child between baseline and 12-month follow-up.
Baseline to 12 months
Number of newly decayed surfaces
Tidsram: Baseline to 12 months
The change in the total number of decayed surfaces (ICDAS codes 1-6, including early enamel lesions) per child between baseline and 12-month follow-up.
Baseline to 12 months
Number of newly cavitated surfaces
Tidsram: Baseline to 12 months
The change in the number of cavitated surfaces (ICDAS codes 3-6, with dentin exposure) per child between baseline and 12-month follow-up.
Baseline to 12 months

Samarbetspartners och utredare

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Studieavstämningsdatum

Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.

Studera stora datum

Studiestart (Faktisk)

1 januari 2023

Primärt slutförande (Faktisk)

1 juni 2024

Avslutad studie (Faktisk)

1 september 2024

Studieregistreringsdatum

Först inskickad

29 april 2026

Först inskickad som uppfyllde QC-kriterierna

7 maj 2026

Första postat (Faktisk)

12 maj 2026

Uppdateringar av studier

Senaste uppdatering publicerad (Faktisk)

12 maj 2026

Senaste inskickade uppdateringen som uppfyllde QC-kriterierna

7 maj 2026

Senast verifierad

1 maj 2026

Mer information

Termer relaterade till denna studie

Andra studie-ID-nummer

  • QYFYWZLL29924

Läkemedels- och apparatinformation, studiedokument

Studerar en amerikansk FDA-reglerad läkemedelsprodukt

Nej

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Nej

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