search
Back to results

Efficacy of Hydrogen Peroxide Gel on Periodontitis With Diabetes (Peroxide gel)

Primary Purpose

Periodontitis, Diabetes Mellitus

Status
Not yet recruiting
Phase
Early Phase 1
Locations
Study Type
Interventional
Intervention
PerioProtect ™= plastic tray +1.7% hydrogen peroxide
Sponsored by
University of Oklahoma
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Periodontitis focused on measuring non surgical periodontal therapy, scaling and root planing

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria: Adults >18 , <80 year old with moderate to severe periodontitis as defined by the Word workshop criteria having Type II diabetes mellitus with HbA1 C levels of >6.5%. No SRP within the past 6 months. Willingness to comply with study instructions and refrain from using oral hygiene products/ procedures outside the study. Exclusion Criteria: The researcher believes that it is not in the patient's best interest to stay in the study Based on the exclusion criteria, the patient becomes ineligible to participate Patient's medical condition requires interventions which preclude involvement in the study Patient does not follow study related instructions The study is suspended or canceled

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    No Intervention

    Experimental

    Arm Label

    Control group

    Test group

    Arm Description

    Will receive SRP alone.

    Will receive SRP + PerioProtect ™.

    Outcomes

    Primary Outcome Measures

    Change of HbA1C measured in percentage.
    To investigate the efficacy of locally delivered 1.7% hydrogen peroxide gel (Perio Gel®)as an adjunct to mechanical periodontal therapy on glycemic control in periodontitis patients with Type 2 diabetes mellitus.
    Change of HbA1C measured in percentage.
    To investigate the efficacy of locally delivered 1.7% hydrogen peroxide gel (Perio Gel®)as an adjunct to mechanical periodontal therapy on glycemic control in periodontitis patients with Type 2 diabetes mellitus.
    Change of HbA1C measured in percentage.
    To investigate the efficacy of locally delivered 1.7% hydrogen peroxide gel (Perio Gel®)as an adjunct to mechanical periodontal therapy on glycemic control in periodontitis patients with Type 2 diabetes mellitus.
    Change of HbA1C measured in percentage.
    To investigate the efficacy of locally delivered 1.7% hydrogen peroxide gel (Perio Gel®)as an adjunct to mechanical periodontal therapy on glycemic control in periodontitis patients with Type 2 diabetes mellitus.

    Secondary Outcome Measures

    Change in Probing Pocket Depth(mm)
    To determine if the use of PerioProtect ™ as an adjunct to mechanical therapy produces additional improvement in periodontal status as compared to conventional periodontal therapy (SRP) alone.
    Change in Bleeding On Probing(%)
    To determine if the use of PerioProtect ™ as an adjunct to mechanical therapy produces additional improvement in periodontal status as compared to conventional periodontal therapy (SRP) alone.
    Change in Plaque Index (0-3).
    To determine if the use of PerioProtect ™ as an adjunct to mechanical therapy produces additional improvement in periodontal status as compared to conventional periodontal therapy (SRP) alone.
    Change in Clinical attachment levels(mm).
    To determine if the use of PerioProtect ™ as an adjunct to mechanical therapy produces additional improvement in periodontal status as compared to conventional periodontal therapy (SRP) alone.

    Full Information

    First Posted
    December 6, 2022
    Last Updated
    December 19, 2022
    Sponsor
    University of Oklahoma
    Collaborators
    Perio Protect LLC
    search

    1. Study Identification

    Unique Protocol Identification Number
    NCT05669560
    Brief Title
    Efficacy of Hydrogen Peroxide Gel on Periodontitis With Diabetes
    Acronym
    Peroxide gel
    Official Title
    Efficacy of Hydrogen Peroxide Gel on Periodontal Ststus and Metabolic Control in Diabetic Patients: a Randomized Control Trial
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    December 2022
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    January 20, 2023 (Anticipated)
    Primary Completion Date
    May 30, 2027 (Anticipated)
    Study Completion Date
    June 30, 2027 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    University of Oklahoma
    Collaborators
    Perio Protect LLC

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    Yes
    Product Manufactured in and Exported from the U.S.
    Yes
    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    Periodontitis is a chronic infectious disease characterized by loss of tooth supporting periodontal structures and alveolar bone. In the U.S. and worldwide, periodontitis is the major cause of tooth loss in adults. Type 2 Diabetes mellitus (T2DM) is a complex disease that affects 13-15 million Americans and is associated with a variety of serious complications. T2DM is well established as a strong systemic risk factor for periodontitis. The severity and prevalence of periodontitis is much higher in patients with diabetes. This relationship may be bi-directional.
    Detailed Description
    The primary treatment for periodontitis is scaling and root planing (SRP), which refers to the mechanical disruption and removal of bacteria and bacterial toxins from the affected tooth root surfaces. This procedure predictably reduces the bacterial load and produces marked improvement in clinical periodontal parameters, though not always complete resolution of the disease. Periodontal therapy may have some systemic benefits by reducing entry into the systemic circulation of pro inflammatory molecules and bacterial byproducts from the periodontal tissues. Since SRP alone is not always a completely effective treatment especially in advanced stages of periodontitis, a variety of adjunctive antimicrobial therapies such as local delivery of antimicrobial agents into periodontal pockets have been developed and employed to further reduce the bacterial load from periodontal pockets, with mixed results. A recent innovation in the arena of local delivery antimicrobial agents is the PerioProtect ™ system (Perio Tray® and PerioGel® Perio Protect, St. Louis, MO). This consists of a closely fitting acrylic tray (similar to an athletic mouthguard), which is used to administer 1.7% hydrogen peroxide gel (Perio Gel®, QNT Anderson, Bismarck, ND) deep into the periodontal pocket and retain the gel in place for a sufficient time period (15 minutes) to effectively reduce the periodontal bacterial load. Studies to date have shown that when PerioProtect ™ is used as adjunct to conventional SRP, this system produces additional benefits in reducing the severity of periodontal disease. However, no studies have yet investigated the use of PerioProtect ™ in patients with T2DM and periodontitis. Based on the concept of a bi-directional relationship of diabetes and periodontitis, the investigators hypothesize that successful management of periodontal infection in diabetics with the use of PerioProtect ™ will not only improve periodontal status, but also result in improved metabolic control of T2DM.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Periodontitis, Diabetes Mellitus
    Keywords
    non surgical periodontal therapy, scaling and root planing

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Early Phase 1
    Interventional Study Model
    Parallel Assignment
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    60 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Control group
    Arm Type
    No Intervention
    Arm Description
    Will receive SRP alone.
    Arm Title
    Test group
    Arm Type
    Experimental
    Arm Description
    Will receive SRP + PerioProtect ™.
    Intervention Type
    Combination Product
    Intervention Name(s)
    PerioProtect ™= plastic tray +1.7% hydrogen peroxide
    Intervention Description
    Subjects will receive PerioProtect ™ in adjunct to mechanical therapy. 15minutes, twice a day, for 3 months.
    Primary Outcome Measure Information:
    Title
    Change of HbA1C measured in percentage.
    Description
    To investigate the efficacy of locally delivered 1.7% hydrogen peroxide gel (Perio Gel®)as an adjunct to mechanical periodontal therapy on glycemic control in periodontitis patients with Type 2 diabetes mellitus.
    Time Frame
    Measured at baseline
    Title
    Change of HbA1C measured in percentage.
    Description
    To investigate the efficacy of locally delivered 1.7% hydrogen peroxide gel (Perio Gel®)as an adjunct to mechanical periodontal therapy on glycemic control in periodontitis patients with Type 2 diabetes mellitus.
    Time Frame
    Measured at 3 months
    Title
    Change of HbA1C measured in percentage.
    Description
    To investigate the efficacy of locally delivered 1.7% hydrogen peroxide gel (Perio Gel®)as an adjunct to mechanical periodontal therapy on glycemic control in periodontitis patients with Type 2 diabetes mellitus.
    Time Frame
    Measured at 6 months
    Title
    Change of HbA1C measured in percentage.
    Description
    To investigate the efficacy of locally delivered 1.7% hydrogen peroxide gel (Perio Gel®)as an adjunct to mechanical periodontal therapy on glycemic control in periodontitis patients with Type 2 diabetes mellitus.
    Time Frame
    Measured at 9 months
    Secondary Outcome Measure Information:
    Title
    Change in Probing Pocket Depth(mm)
    Description
    To determine if the use of PerioProtect ™ as an adjunct to mechanical therapy produces additional improvement in periodontal status as compared to conventional periodontal therapy (SRP) alone.
    Time Frame
    Measured at baseline, 3, 6, 9months.
    Title
    Change in Bleeding On Probing(%)
    Description
    To determine if the use of PerioProtect ™ as an adjunct to mechanical therapy produces additional improvement in periodontal status as compared to conventional periodontal therapy (SRP) alone.
    Time Frame
    Measured at baseline, 3, 6, 9months.
    Title
    Change in Plaque Index (0-3).
    Description
    To determine if the use of PerioProtect ™ as an adjunct to mechanical therapy produces additional improvement in periodontal status as compared to conventional periodontal therapy (SRP) alone.
    Time Frame
    Measured at baseline, 3, 6, 9months.
    Title
    Change in Clinical attachment levels(mm).
    Description
    To determine if the use of PerioProtect ™ as an adjunct to mechanical therapy produces additional improvement in periodontal status as compared to conventional periodontal therapy (SRP) alone.
    Time Frame
    Measured at baseline, 3, 6, 9months.

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Maximum Age & Unit of Time
    80 Years
    Accepts Healthy Volunteers
    Accepts Healthy Volunteers
    Eligibility Criteria
    Inclusion Criteria: Adults >18 , <80 year old with moderate to severe periodontitis as defined by the Word workshop criteria having Type II diabetes mellitus with HbA1 C levels of >6.5%. No SRP within the past 6 months. Willingness to comply with study instructions and refrain from using oral hygiene products/ procedures outside the study. Exclusion Criteria: The researcher believes that it is not in the patient's best interest to stay in the study Based on the exclusion criteria, the patient becomes ineligible to participate Patient's medical condition requires interventions which preclude involvement in the study Patient does not follow study related instructions The study is suspended or canceled
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Jaewon Kim, DDS, MSD, PhD
    Phone
    716 604 4064
    Email
    Jaewon-Kim@ouhsc.edu
    First Name & Middle Initial & Last Name or Official Title & Degree
    Madhumati Ramachandrareddy, DDS
    Phone
    470 364 0595
    Email
    madhumati-ramachandrareddy@ouhsc.edu
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    John Dmytryk, DDS, PhD
    Organizational Affiliation
    The University of Oklahoma, College of Dentistry, Division in Periodontics
    Official's Role
    Study Chair

    12. IPD Sharing Statement

    Plan to Share IPD
    Undecided

    Learn more about this trial

    Efficacy of Hydrogen Peroxide Gel on Periodontitis With Diabetes

    We'll reach out to this number within 24 hrs