FindMyKOL
Clinical trialNCT00997178CompletedPhase 3Interventional

Diabetes and Periodontal Therapy Trial

SponsorStony Brook UniversityEnrollment514Chronic PeriodontitisType 2 Diabetes
View the registry record on ClinicalTrials.gov

Summary

The lay summary the sponsor registered on ClinicalTrials.gov.

The primary aim of the study is to determine if non-surgical periodontal therapy (scaling and root planing and supportive periodontal therapy) is efficacious compared to delayed therapy in reducing elevated glycosylated hemoglobin (HbA1c) at 6 months post-randomization in subjects with type 2 diabetes and untreated, moderate to advanced chronic periodontitis. The secondary aims of the study are to: 1. evaluate whether 6 month (or shorter-term (3 month)) changes in clinical measures of chronic periodontitis (gingival index, bleeding on probing, probing depth, clinical attachment level) are related to changes in HbA1c and fasting glucose or insulin resistance as measured by the Homeostasis Model Assessment 2 (HOMA2). 2. assess the 3 month and 6 month efficacy of periodontal therapy on all of the above study outcomes. If a treatment response is observed for any of the study outcomes at 3 months, then the trial can evaluate whether this response is sustained at 6 months.

Investigators

The overall officials registered on this study. Names that resolve to a FindMyKOL profile link to it; the rest are shown as registered.

A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.

Sites

8 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.

United States
  • Clinical Site: University of Alabama at Birmingham

    Birmingham, Alabama, United States

  • Clinical Site: University of Minnesota

    Minneapolis, Minnesota, United States

  • Core Laboratory: University of Minnesota

    Minneapolis, Minnesota, United States

  • Administrative Center/study Chair'S Office: Stony Brook University

    Stony Brook, New York, United States

  • Clinical Site: Stony Brook University

    Stony Brook, New York, United States

  • Coordinating Center: Stony Brook University-

    Stony Brook, New York, United States

  • University of Texas, Health Sciences Center at Houston

    Houston, Texas, United States

  • Clinical Site: University of Texas Health Science Center

    San Antonio, Texas, United States

Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.

Drugs studied

No drug or biological interventions are in our data for this study. It may test a procedure, device or behavioral intervention, or the intervention list isn't in our current snapshot. See the registry record ↗. Why? →

Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start
31 Oct 2009
Primary completion
31 Oct 2012
Completion
31 Dec 2012
Last update posted
20 Jan 2014
Registered enrollment
514
Registry id
NCT00997178

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 11 Nov 2026. Registry facts are shown as registered by the study sponsor; FindMyKOL does not interpret them.