Treating Periodontal Infection: Effects on Glycemic Control in People With Type 2 Diabetes

The recruitment status of this study is unknown because the information has not been verified recently.
Verified October 2007 by National Institute of Dental and Craniofacial Research (NIDCR).
Recruitment status was  Active, not recruiting
Sponsor:
Information provided by:
National Institute of Dental and Craniofacial Research (NIDCR)
ClinicalTrials.gov Identifier:
NCT00016835
First received: June 5, 2001
Last updated: October 5, 2007
Last verified: October 2007

June 5, 2001
October 5, 2007
April 2001
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Complete list of historical versions of study NCT00016835 on ClinicalTrials.gov Archive Site
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Treating Periodontal Infection: Effects on Glycemic Control in People With Type 2 Diabetes
Treating Periodontal Infection: Effects on Glycemic Control

The purpose of this project is to obtain important preliminary data necessary to support design of a full scale, multicenter randomized clinical trial (RCT) to evaluate the effect of treating periodontal infection on glycemic control in type 2 diabetes mellitus.

There is compelling epidemiological and clinical evidence to suggest that periodontal infection adversely affects glycemic control in people with type 2 diabetes mellitus. The purpose of this pilot project is to obtain important preliminary data necessary to support design of a full scale, multi-center randomized clinical trial (RCT) to evaluate the effect of treating periodontal infection on glycemic control in individuals with type 2 diabetes mellitus. This current project involves treating periodontal infection to obtain estimates of changes and the variability of those changes over time in the established primary endpoint, hemoglobin A1c (HbA1c). This project will also explore use of several potential secondary endpoints including levels of periodontitis and glucose metabolism-related inflammatory mediators (TNF-alpha, IL-1-beta, IL-6), serum cholesterol, triglyceride and lipids. Subjects are randomly assigned to 1 of three possible groups for comprehensive periodontal examination, specimen collection, mechanical periodontal therapy and oral systemic antibiotics or placebo, and regular follow-up evaluations and site-specific mechanical periodontal therapy, at 3-month intervals, for approximately 15 months. Two groups receive ultrasonic scaling with local anesthesia (as needed), local antimicrobial treatment with povidone-iodine irrigation, and an oral systemic antibiotic (either doxycycline or metronidazole) at the initial treatment visit. The third group ("controls") receives a placebo and supra-gingival oral prophylaxis and ultrasonic removal of supra-gingival calculus with water irrigation at the initial treatment visit. At the 9-month follow-up visit, "controls" receive sub-gingival ultrasonic scaling with povidone-iodine irrigation.

Results from this pilot project will be used as preliminary data to support design of an immediate follow-up proposal to NIH/NIDCR for funding a multi-center RCT to evaluate the effect of treating periodontal infection on glycemic control in type 2 diabetes. If results from the full scale clinical trial provide evidence that treating periodontal infection contributes to improved glycemic control, then diagnosis and treatment of periodontal infection in subjects with type 2 diabetes could be substantiated as an important component in management of diabetes.

Interventional
Phase 2
Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Single Group Assignment
Masking: Double-Blind
Primary Purpose: Treatment
  • Periodontal Disease
  • Diabetes Mellitus, Non-Insulin-Dependent
  • Procedure: periodontal scaling and local antibiotic irrigation
  • Procedure: systemic antibiotic (either doxycycline or metronidazole).
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*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Active, not recruiting
45
October 2008
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Inclusion Criteria

  • Subjects must be 18 years of age or older,
  • have at least six natural teeth,
  • have established periodontal disease (established at the screening examination),
  • have a history of type 2 diabetes of at least six months with HbAlc > 7.1%.

Exclusion Criteria

  • Subjects will be excluded from the study if they are presently under the care of a periodontist;
  • have had antibiotic treatment within the previous three months;
  • have conditions that require antibiotic prophylaxis for dental treatment;
  • have allergies to iodine, doxycycline, metronidazole, or chlorhexidine;
  • have blood dyscrasias;
  • are pregnant or breast feeding;
  • have severe cognitive or communication impairment;
  • have a cardiac pacemaker;
  • are under cancer chemotherapy;
  • are medically unstable or have a life expectancy of less than two years;
  • are currently taking disulfiram, phenobarbital, lithium, terfenadine, astemizole, or warfarin;
  • or are out of town or otherwise unavailable for more than three consecutive months of the year.
Both
18 Years and older
No
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT00016835
NIDCR-03, R01 DE13796
Yes
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National Institute of Dental and Craniofacial Research (NIDCR)
Not Provided
Principal Investigator: George W. Taylor, DMD, Dr.PH University of Michigan
National Institute of Dental and Craniofacial Research (NIDCR)
October 2007

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP