FISSURE: Occlusal Caries Management in First Permanent Molars in Child Dental Care

Sponsor
Oral Health Centre of Expertise in Eastern Norway (Other)
Overall Status
Active, not recruiting
CT.gov ID
NCT03315312
Collaborator
Public Dental Service, Hedmark (Other), Public Dental Service, Oppland (Other), Public Dental Service, Østfold (Other)
410
1
2
82.9
4.9

Study Details

Study Description

Brief Summary

Occlusal caries management in first permanent molars: a pragmatic randomized clinical trial in child dental care

Aim of the present study is to evaluate the effectiveness of fissure sealants and fluoride varnish in a pragmatic randomized clinical trial and evaluate whether some specific patient groups benefit more from any particular treatment.

The high risk children (having a previous caries experience at 5 years of age) from 2009, 2010 and 2011 birth cohorts (6-, 7- and 8-year-olds) from three counties (Østfold, Oppland and Hedmark) are selected. Children with at least two erupted first permanent molars in the same jaw randomly receive resin-based sealant or a fluoride varnish (Duraphat) during a routine dental examination. Children who already developed caries, had restorations or fissure sealants placed in first molars were excluded from the present study.

Fluoride varnish and resin-based fissure sealants are randomly applied on contra-lateral teeth where each child serves as its own control. This study uses a natural clinical setting, where clinicians use methods and procedures that are routinely applied in public dental clinics. The study is approved by the Regional Committee for Medical Research Ethics South East (2016/2002/REK sør-øst C).

Sample size calculations: Based on the assumption that 80% of the treated teeth do not get caries and that 10% difference in caries development constitutes a clinically meaningful difference, it is required to recruit 180 participants in the study for the split-mouth design. Considering a potential maximum of annual 20% drop-out rate and a 3-years follow-up, the study will need to recruit 400 participants in order to have at least 206 children at the 3 years of follow-up.

Treatments are provided by either dentists or dental hygienists during routine dental examinations. Caregivers of eligible children are informed about the study, the participation is voluntary and an informed written parental consent is obtained in accordance with the directions of the Regional Committee for Medical Research Ethics. In this study, a clinician selects a random treatment for the first tooth by choosing one of the two cards, while a collateral tooth receives an alternative treatment. Subsequently, treatments provided and materials used are recorded on a treatment registration form. During this study, clinicians follow their conventional clinical procedures for applying sealants or fluoride varnish. Information on patient's caries experience and quality of oral hygiene are recorded on treatment registration form. Fluoride varnish is applied three times, at baseline, 6 months and 12 months.

Caries on occlusal surfaces of first molars detected at later 24 and 36 months follow-ups will be recorded in the follow-up registration form. The main study outcome is caries occurrence on occlusal tooth surfaces.

Condition or Disease Intervention/Treatment Phase
  • Drug: Fluoride Varnishes
  • Drug: Fissure Sealants
Phase 4

Study Design

Study Type:
Interventional
Actual Enrollment :
410 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Split-mouth designSplit-mouth design
Masking:
None (Open Label)
Primary Purpose:
Prevention
Official Title:
FISSURE-Project. Improved Dental Decay Management in Dental Service for Children: Fissure Sealants or Fluoride Varnish?
Actual Study Start Date :
Feb 1, 2017
Anticipated Primary Completion Date :
Dec 31, 2022
Anticipated Study Completion Date :
Dec 31, 2023

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Fissure sealant

Drug: Fissure Sealants
Resin-based fissure sealant is applied on contra-lateral first permanent molar and each child serves as its own control. This study uses a natural clinical setting, where clinicians use methods and procedures that are routinely applied in public dental clinics.

Experimental: Fluoride varnish

Drug: Fluoride Varnishes
Fluoride varnish is randomly applied on randomly selected first permanent molar. This study uses a natural clinical setting, where clinicians use methods and procedures that are routinely applied in public dental clinics.

Outcome Measures

Primary Outcome Measures

  1. Dental caries incidence on occlusal surfaces of first molars [12 months after application]

    Decayed, missing and filled surfaces (DMFS) increment

  2. Dental caries incidence on occlusal surfaces of first molars [24 months after application]

    Decayed, missing and filled surfaces (DMFS) increment

  3. Dental caries incidence on occlusal surfaces of first molars [36 months after application]

    Decayed, missing and filled surfaces (DMFS) increment

Eligibility Criteria

Criteria

Ages Eligible for Study:
6 Years to 9 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • The high risk children (having a previous caries experience at 5 years of age) with at least two erupted first permanent molars
Exclusion Criteria:
  • Children who already developed caries, had restorations or fissure sealants placed in first molars are excluded from the present study.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Public Dental Service clinics at Østfold county Sarpsborg Norway

Sponsors and Collaborators

  • Oral Health Centre of Expertise in Eastern Norway
  • Public Dental Service, Hedmark
  • Public Dental Service, Oppland
  • Public Dental Service, Østfold

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Oral Health Centre of Expertise in Eastern Norway
ClinicalTrials.gov Identifier:
NCT03315312
Other Study ID Numbers:
  • FISSURE
First Posted:
Oct 20, 2017
Last Update Posted:
Sep 8, 2021
Last Verified:
Sep 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
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 8, 2021