Treating Periodontal Infection: Effects on Glycemic

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

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.

Study Overview

• Status: Completed
• Conditions: Diabetes Mellitus, Type 2; Periodontal Disease
• Intervention / Treatment: Procedure: Supra-gingival scaling and placebo; Procedure: Subgingival scaling and metronidazole; Procedure: Subgingival scaling and doxycycline

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.

• Study Type: Interventional
• Enrollment (Actual): 46
• Phase: Phase 2

Contacts and Locations

Study Locations

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

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years and older (Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

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.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: Double

Number of Arms

3

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Active Comparator: Supra-gingival scaling and placebo; This group receives a placebo (instead of systemic antibiotic), 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, this group will receive sub-gingival ultrasonic scaling with povidone-iodine irrigation. This group also receives regular follow-up evaluations and site-specific mechanical periodontal therapy, at 3-month intervals, for approximately 15 months.	Procedure: Supra-gingival scaling and placebo; Included in arm/group description.
Experimental: Subgingival scaling and metronidazole; This group receives ultrasonic scaling with local anesthesia (as needed), local antimicrobial treatment with povidone-iodine irrigation, and metronidazole as an oral systemic antibiotic at the initial treatment visit. This group also receives regular follow-up evaluations and site-specific mechanical periodontal therapy, at 3-month intervals, for approximately 15 months.	Procedure: Subgingival scaling and metronidazole; Included in arm/group description.
Experimental: Subgingival scaling and doxycycline; This group receives ultrasonic scaling with local anesthesia (as needed), local antimicrobial treatment with povidone-iodine irrigation, and doxycycline as an oral systemic antibiotic at the initial treatment visit. This group also receives regular follow-up evaluations and site-specific mechanical periodontal therapy, at 3-month intervals, for approximately 15 months.	Procedure: Subgingival scaling and doxycycline; Included in arm/group description.

Collaborators and Investigators

• Sponsor: University of Michigan
• Collaborators: National Institute of Dental and Craniofacial Research (NIDCR)
• Investigators: Principal Investigator: George W. Taylor, DMD, Dr.PH, University of Michigan

Study record dates

Study Major Dates

• Study Start (Actual): October 17, 2001
• Primary Completion (Actual): September 3, 2004
• Study Completion (Actual): September 3, 2004

Study Registration Dates

• First Submitted: June 5, 2001
• First Submitted That Met QC Criteria: June 6, 2001
• First Posted (Estimate): June 7, 2001

Study Record Updates

• Last Update Posted (Actual): July 19, 2017
• Last Update Submitted That Met QC Criteria: July 14, 2017
• Last Verified: July 1, 2017

More Information

Terms related to this study

• Keywords: Type 2 diabetes mellitus; Glycemic control; Periodontal therapy
• Additional Relevant MeSH Terms: Glucose Metabolism Disorders; Metabolic Diseases; Endocrine System Diseases; Stomatognathic Diseases; Mouth Diseases; Diabetes Mellitus; Diabetes Mellitus, Type 2; Periodontal Diseases; Anti-Infective Agents; Anti-Bacterial Agents; Antiprotozoal Agents; Antiparasitic Agents; Antimalarials; Metronidazole; Doxycycline
• Other Study ID Numbers: NIDCR-03; 5R01DE013796-03 (U.S. NIH Grant/Contract)

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: NO
• IPD Plan Description: There is no current plan to share data with other researchers at this time