Effectiveness of Pit and Fissure Sealants in the Prevention of Dental Caries

Sponsor
Centre Hospitalier Universitaire de Nice (Other)
Overall Status
Completed
CT.gov ID
NCT00674869
Collaborator
(none)
400
1
2
48
8.3

Study Details

Study Description

Brief Summary

This randomized clinical trial is aimed at testing the efficacy of pit and fissure sealants, in a current environmental context different from that of the seventies and eighties. It has a split mouth design. 4OO subjects are included and the duration of follow up is 2 years.

Condition or Disease Intervention/Treatment Phase
  • Other: pit and fissure sealant
N/A

Detailed Description

This randomized clinical trial is aimed at testing the efficacy of pit and fissure sealants, in a current environmental context different from that of the seventies and eighties. This study assesses the cost-effectiveness of sealants according to the individual caries risk. This study takes place in Nice, Marseille and Paris (France) and the patients are to be enrolled both in the dental hospitals and in the private practice. In the hospitals, the subjects are recruited directly by the headmasters of the pediatric dentistry or public health departments in the three dental schools. In private practice, the head of the department of pediatric dentistry and / or public health dentistry, of each dental school chooses 4 to 6 private practitioners who are used to place dental sealants in their daily practice. They recruit the subjects among their own patients. The type of study corresponds to randomized clinical trial (Split mouth design) in which the tooth is the statistical unit (one pair of molars considered for each included patient). This study has a direct benefit for individuals. The number of necessary subjects is 328; the sample size is 400. The follow-up duration is 2 years. The treatment is a pit and fissure sealant on one randomized tooth by pair of permanent molars (Split mouth design). Sealant material is set up in accordance with the usual practice of each practitioner. Occlusal exams are conducted every 6 months. The effectiveness of dental sealants and the retention of sealing materials are statistically analyzed according to both the individual caries risk and the clinical protocol

Study Design

Study Type:
Interventional
Actual Enrollment :
400 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Prevention
Official Title:
Effectiveness of Pit and Fissure Sealants in the Prevention of Dental Caries
Study Start Date :
Dec 1, 2004
Actual Primary Completion Date :
Dec 1, 2008
Actual Study Completion Date :
Dec 1, 2008

Arms and Interventions

Arm Intervention/Treatment
Experimental: 1

pit and fissure sealant on one randomized tooth by pair of permanent molar

Other: pit and fissure sealant
pit and fissure sealant on one randomized tooth by pair of permanent molar

No Intervention: 2

No intervention

Outcome Measures

Primary Outcome Measures

  1. Caries development [every six month during 2 years]

Secondary Outcome Measures

  1. CAOD [every six months during 2 years]

  2. Retention sealing of furrows (grooves) [every 6 months during 2 years]

Eligibility Criteria

Criteria

Ages Eligible for Study:
6 Years to 15 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • child over 6 years old

  • patient with at least one carie

  • patient with at least one pair of permanent molar: healthy or with equivalent injuries

Exclusion Criteria:
  • not cooperating in care

  • not speaking french or english

Contacts and Locations

Locations

Site City State Country Postal Code
1 Centre Hospitalier Universitaire de Nice Nice France 06000

Sponsors and Collaborators

  • Centre Hospitalier Universitaire de Nice

Investigators

  • Principal Investigator: Michèle Muller-Bolla, Pr, Service d'Odontologie

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Centre Hospitalier Universitaire de Nice
ClinicalTrials.gov Identifier:
NCT00674869
Other Study ID Numbers:
  • 03-APR-12
First Posted:
May 8, 2008
Last Update Posted:
Feb 22, 2012
Last Verified:
Jun 1, 2009
Keywords provided by Centre Hospitalier Universitaire de Nice
Additional relevant MeSH terms:

Study Results

No Results Posted as of Feb 22, 2012