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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00847470
Other study ID # 101883
Secondary ID
Status Completed
Phase N/A
First received February 17, 2009
Last updated November 17, 2014
Start date June 2006
Est. completion date December 2008

Study information

Verified date November 2014
Source Dental Practice-Based Research Network
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

Clinical Trial Summary

The purpose of this study was to document the reasons for placing the first restoration ("filling") on a previously un-restored surface in a permanent ("adult") tooth.


Description:

The aims of this study were to (1) quantify DPBRN practitioner-investigators pre-operative and post-operative assessments of the depth of the caries lesion being treated; (2) quantify the prevalence of dental material types used to restore the first restoration in a permanent tooth surface; and (3) test the hypothesis that DPBRN practitioner investigators in the "Assessment of caries diagnosis and caries treatment" study who stated that they wait until the caries lesions reach dentin before they place the first restoration are in fact more likely in this study to do restoration in teeth that have caries reaching into dentin.

The aims were met by enrolling 230 DPBRN practitioner-investigators in the "Reasons for placing the first restoration on permanent tooth surfaces" study, each of whom recorded information about approximately 50 consecutive restorations that they placed on unrestored surfaces. This study about restorative treatment received by patients provided the opportunity to record the variations in the treatment provided, and also provided a basis for subsequent future studies to investigate how defects on fillings develop over time. These results will also be related to the findings from "Assessment of caries diagnosis and caries treatment" study where practitioners outlined how they detected dental decay, the stage at which the decay was treated by placing fillings, and how they rely on preventive measures to stop the decay process without placing fillings.


Recruitment information / eligibility

Status Completed
Enrollment 5810
Est. completion date December 2008
Est. primary completion date December 2008
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 6 Years and older
Eligibility Inclusion Criteria:

- participants directly involved in this study were patients who sought dental treatment in the practitioner-investigators' practices

- any tooth surface that was previously unrestored was eligible for this study, provided that it was on a permanent ("adult") tooth. This means that permanent first molars were eligible, which typically erupt at about age 6 years. This means that persons age 6 and older were enrolled in the study and there was no upper age limit.

Exclusion Criteria:

Study Design

Time Perspective: Cross-Sectional


Related Conditions & MeSH terms


Locations

Country Name City State
Denmark University of Copenhagen Royal Dental College Copenhagen
United States University of Alabama at Birmingham Birmingham Alabama
United States University of Florida College of Dentistry Gainesville Florida
United States Health Partners Dental Group Minneapolis Minnesota
United States Health Partners Research Foundation Minneapolis Minnesota
United States Kaiser Permanente Center for Health Research Portland Oregon
United States Permanente Denrtal Associates Portland Oregon

Sponsors (7)

Lead Sponsor Collaborator
Dental Practice-Based Research Network HealthPartners Institute, Kaiser Permanente, Permanente Dental Associates Group, Oregon, University of Copenhagen, University of Florida, University of North Carolina, Chapel Hill

Countries where clinical trial is conducted

United States,  Denmark, 

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