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OpenTrials
Completed

NCT Number: NCT01768390

Caries-preventive Effect of a Dentifrice Containing 5,000 Ppm Fluoride in Orthodontic Patients

AIM: To evaluate the efficacy of daily tooth brushing with high concentrated fluoride dentifrice on white spot lesion (WSL) formation in adolescents during treatment with fixed orthodontic appliances (FOA).

The null hypothesis is that neither incidence nor severity of lesions would differ from a control group using standard fluoride dentifrice.

SUBJECTS AND METHODS: 420 healthy consecutive 11-16 year-old patients referred to 4 Orthodontic Specialist Clinics are randomized to use either a dentifrice containing 5.000 ppm fluoride or a regular dentifrice with 1.450 ppm sodium fluoride. To be eligible for inclusion, the patients are scheduled for bimaxillary treatment with FOA for an expected duration of at least 1 year. All are instructed to use 0.25 gram dentifrice and brush their teeth during 2 minutes twice daily during the entire period of treatment. Before bonding, and after polishing with a rubber cup and non-fluoride pumice paste, 3 digital photos of the maxillary incisors, canines and premolars are taken. At debonding, remaining composite material on the surfaces is removed with a slow rotating carbide bur followed by polishing with a rubber cup and pumice paste. A new series of frontal and lateral digital photos is thereafter exposed.

The primary outcome measure is the incidence and severity of WSL as registered separately by two blinded experienced and calibrated clinicians according to a validated index. A random sample of 50 cases is re-assessed to check intra- and inter-examiner reliability. The intervention is indended run throughout the full duration of the orthodontic treatment, varying between 18 and 24 months.

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Key information

Age range

11 year–16 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Halland Hospital

Halmstad, 30185, Sweden

About this study

not desired

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • healthy
  • bi-maxillary treatment with fixed orthodontic appliances for at least 1 year

Exclusion criteria

  • poor oral hygiene (not being able to brush their teeth)
  • recent high caries activity

Treatment and study plan

toothpaste containing 5,000 ppm fluoride

Other

1 cm tootpaste twice daily during 2 minutes

1450 GCP

Other

Twice gaily toothbrushing with normal adult toothpaste containing 1450 ppm F representing good clinical practice

Primary outcomes

  1. White spot lesion incidence

    Time frame: up to 24 months (at debonding of ortodontic appliances)

    Clinical scoring according to validated index

Secondary outcomes

  1. white spot lesion severity

    Time frame: up to 24 months (at debonding of orthodontic brackets)

    clinical scoring according to a validated index

Sponsors and collaborators

Lead sponsor

University of Copenhagen

Other

Registry information

Official study title

Caries-preventive Effectiveness of a Dentifrice Containing 5.000 Ppm Fluoride - a Randomized Controlled Trial in Adolescents With Fixed Orthodontic Appliances

Important dates

Study start
2008
Primary completion
2012
Study completion
2012
First posted
Jan 15, 2013
Registry last updated
Jan 15, 2013

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.

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