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

This study is ongoing, but not recruiting participants.

Sponsored by: National Institute of Dental and Craniofacial Research (NIDCR)
Information provided by: National Institute of Dental and Craniofacial Research (NIDCR)
ClinicalTrials.gov Identifier: NCT00016835
  Purpose

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.


Condition Intervention Phase
Periodontal Disease
Diabetes Mellitus, Non-Insulin-Dependent
Procedure: periodontal scaling and local antibiotic irrigation
Procedure: systemic antibiotic (either doxycycline or metronidazole).
Phase II

MedlinePlus related topics:   Antibiotics    Diabetes   

Drug Information available for:   Doxycycline    Doxycycline calcium    Doxycycline hyclate    Metronidazole    Metronidazole hydrochloride    Metronidazole phosphate   

U.S. FDA Resources

Study Type:   Interventional
Study Design:   Treatment, Randomized, Double-Blind, Active Control, Single Group Assignment, Efficacy Study
Official Title:   Treating Periodontal Infection: Effects on Glycemic Control

Further study details as provided by National Institute of Dental and Craniofacial Research (NIDCR):

Estimated Enrollment:   45
Study Start Date:   April 2001
Estimated Study Completion Date:   October 2008

Detailed Description:

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.

  Eligibility
Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No

Criteria

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.
  Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00016835

Locations
United States, Michigan
Department of Cariology, Restorative Sciences and Endodontics    
      Ann Arbor, Michigan, United States, 48109-1078

Sponsors and Collaborators

Investigators
Principal Investigator:     George W. Taylor, DMD, Dr.PH     University of Michigan    
  More Information


Study ID Numbers:   NIDCR-03, R01 DE13796
First Received:   June 5, 2001
Last Updated:   October 5, 2007
ClinicalTrials.gov Identifier:   NCT00016835
Health Authority:   United States: Federal Government

Keywords provided by National Institute of Dental and Craniofacial Research (NIDCR):
Type 2 diabetes mellitus  

Study placed in the following topic categories:
Mouth Diseases
Metronidazole
Periodontal Diseases
Metabolic Diseases
Diabetes Mellitus, Type 2
Diabetes Mellitus
Endocrine System Diseases
Endocrinopathy
Stomatognathic Diseases
Metabolic disorder
Glucose Metabolism Disorders
Doxycycline

Additional relevant MeSH terms:
Antimalarials
Anti-Infective Agents
Anti-Bacterial Agents
Antiparasitic Agents
Antiprotozoal Agents
Radiation-Sensitizing Agents
Therapeutic Uses
Physiological Effects of Drugs
Pharmacologic Actions

ClinicalTrials.gov processed this record on December 03, 2008




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