DPBRN Blood Sugar Testing in Dental Patients
Blood Sugar Testing in Dental Patients
2 other identifiers
observational
498
2 countries
7
Brief Summary
The principal goal of this study was to assess the feasibility of plasma glucose testing in private dental practice. A second aim was was to assess prevalence of plasma glucose abnormalities in dental patients seen by (DPBRN) practitioner-investigators.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Apr 2009
7 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
April 1, 2009
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 1, 2010
CompletedStudy Completion
Last participant's last visit for all outcomes
July 1, 2010
CompletedFirst Submitted
Initial submission to the registry
September 13, 2010
CompletedFirst Posted
Study publicly available on registry
September 14, 2010
CompletedJune 16, 2011
June 1, 2011
1.2 years
September 13, 2010
June 14, 2011
Conditions
Keywords
Study Arms (1)
Glucose testing
Patients participating in this study may be alerted to possible presence of (DM) or pre-(DM) or to inadequate glycemic control. In such a case, they were advised to follow-up with their physician for definitive diagnosis and treatment. Early diagnosis and improved glycemic control may be of significant benefit to the patients' health.
Eligibility Criteria
The human subjects direclty involved in this study were the patients who had sought dental treatment in the (DPBRN) practitioner-investigators' practices.
You may qualify if:
- adults over the age of 19 who were scheduled for a visit with an exam
You may not qualify if:
- patients undergoing continuing treatment where an exam was not part of the visit were not eligible
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Dental Practice-Based Research Networklead
- National Institute of Dental and Craniofacial Research (NIDCR)collaborator
- HealthPartners Institutecollaborator
- Kaiser Permanentecollaborator
- Permanente Dental Associates Group, Oregoncollaborator
Study Sites (7)
University of Alabama at Birmingham
Birmingham, Alabama, 35294, United States
University of Florida College of Dentistry
Gainesville, Florida, 32610, United States
Health Partners Dental Group
Minneapolis, Minnesota, 55440-1309, United States
Health Partners Research Foundation
Minneapolis, Minnesota, 55440-1524, United States
Kaiser Permanente Center for Health Research
Portland, Oregon, 97227, United States
Permanente Denrtal Associates
Portland, Oregon, 97232, United States
University of Copenhagen Royal Dental College
Copenhagen, Denmark
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Andrei Barasch, DMD, MDSc
The University of Alabama at Birmingham
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- CROSS SECTIONAL
- Sponsor Type
- NETWORK
Study Record Dates
First Submitted
September 13, 2010
First Posted
September 14, 2010
Study Start
April 1, 2009
Primary Completion
July 1, 2010
Study Completion
July 1, 2010
Last Updated
June 16, 2011
Record last verified: 2011-06