Treating Periodontal Infection: Effects on Glycemic

Sponsor

University of Michigan (Other)

Overall Status

Completed

CT.gov ID

NCT00016835

Collaborator

National Institute of Dental and Craniofacial Research (NIDCR) (NIH)

Enrollment

Location

Arms

34.6

Actual Duration (Months)

1.3

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

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 or Disease	Intervention/Treatment	Phase
Periodontal Disease Diabetes Mellitus, Type 2	Procedure: Supra-gingival scaling and placebo Procedure: Subgingival scaling and metronidazole Procedure: Subgingival scaling and doxycycline	Phase 2

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 Design

Study Type:

Interventional

Actual Enrollment :

46 participants

Allocation:

Randomized

Intervention Model:

Parallel Assignment

Intervention Model Description:

Study participants were randomized into 3 groups for the initial non-surgical treatment appointment. One group received supra-gingival scaling and placebo, one group received non-surgical periodontal supra- and sub-gingival scaling plus metronidazole and one group received non-surgical periodontal supra- and sub-gingival scaling plus doxycycline. All three groups received 3-month follow-up visits for 15 months and the group receiving supra-gingival scaling and placebo at the initial visit received supra- and sub-gingival scaling at the 9-month follow-up visit.Study participants were randomized into 3 groups for the initial non-surgical treatment appointment. One group received supra-gingival scaling and placebo, one group received non-surgical periodontal supra- and sub-gingival scaling plus metronidazole and one group received non-surgical periodontal supra- and sub-gingival scaling plus doxycycline. All three groups received 3-month follow-up visits for 15 months and the group receiving supra-gingival scaling and placebo at the initial visit received supra- and sub-gingival scaling at the 9-month follow-up visit.

Masking:

Double (Participant, Care Provider)

Masking Description:

Participants and examiners were unaware of the type of medication and examiners were also unaware of the type of periodontal therapy the participants receive

Primary Purpose:

Treatment

Official Title:

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

Actual Study Start Date :

Oct 17, 2001

Actual Primary Completion Date :

Sep 3, 2004

Actual Study Completion Date :

Sep 3, 2004

Arms and Interventions

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.

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.

Outcome Measures

Primary Outcome Measures

Eligibility Criteria

Criteria

Ages Eligible for Study:

18 Years and Older

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

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.