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Periodontal Treatment in Non-controlled Type 2 Diabetes Mellitus Patients. Clinical Trial (FONIS12I2106)

Primary Purpose

Diabetes Mellitus., Chronic Periodontitis

Status
Completed
Phase
Not Applicable
Locations
Chile
Study Type
Interventional
Intervention
conventional periodontal treatment
Sponsored by
Universidad de los Andes, Chile
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Diabetes Mellitus. focused on measuring Diabetes mellitus., Periodontitis, Periodontal treatment.

Eligibility Criteria

30 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Decompensated type 2 diabetic patients (HbA1c ≥ 7% at last check).
  • Minimum 12 teeth in the mouth.
  • no history of surgical or nonsurgical periodontal treatment in the six months prior to baseline.
  • not be involved in another clinical trial.

Exclusion Criteria:

  • Patients with renal failure
  • Patients with rheumatoid arthritis,
  • Patients with heart disease.
  • Patients with history of stroke or acute cardiovascular event in the 12 months prior to the start of the study.
  • Patients with liver dysfunction
  • Patients in state of pregnancy or planning pregnancy.
  • Patients on medical treatment with systemic antibiotics in the past 3 months.

Sites / Locations

  • Joan Alsina Polyclinic

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

conventional periodontal treatment

Intensive periodontal treatment

Arm Description

Treatment group by quadrant in five weeks. Patients in this group will receive periodontal treatment including plaque control instructions, supragingival and subgingival debridement and root planing. This treatment is done in 5 sessions with a periodicity of 1 session per week. In the first session patients will receive hygiene instruction and supragingival debridement performed with and ultrasonic device. In the following session, there will be done the scaling and root planing to one quadrant per session, using site specific hand curettes. In case of being partially edentulous patients will be implemented at least 3 teeth per quadrant in each session.

Intensive treatment group in 24 hours: Patients in this group will receive periodontal treatment including: plaque control instructions, supragingival and subgingival debridement and scaling and root planing. This treatment is carried out in 2 sessions within 24 hours. In the first session hygiene instruction and supragingival and scaling and root planing of the teeth in right side at the upper jaw and mandible will be performed. The implementation of each upper and lower hemiarcade will be made until the periodontist treating check manually the removal of all subgingival calculus deposit and feel the smoothness of the root surface. In the second session, there will be an identical procedure in the arch left.

Outcomes

Primary Outcome Measures

Glycated hemoglobin (HbA1c)
Assess levels and relationship of HbA1c in peripheral blood and gingival crevicular fluid at baseline, 3 and 6 months after periodontal treatment in the group of patients treated by intensive and conventional periodontal treatment.

Secondary Outcome Measures

C-reactive protein
Assess levels and relationship of C-reactive protein, in peripheral blood and gingival crevicular fluid at baseline, 3 and 6 months after periodontal treatment in the group of patients treated by intensive and conventional periodontal treatment .
Interleukin-6 (IL-6)
Assess levels and relationship of IL-6 in peripheral blood and gingival crevicular fluid at baseline, 3 and 6 months after periodontal treatment in the group of patients treated by intensive and conventional treatment.
Tumor Necrosis Factor (TNF)
Asses levels and relationship of TNF in peripheral blood and gingival crevicular fluid at baseline, 3 and 6 months after intensive and conventional periodontal treatment.

Full Information

First Posted
July 14, 2013
Last Updated
December 15, 2015
Sponsor
Universidad de los Andes, Chile
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1. Study Identification

Unique Protocol Identification Number
NCT01904422
Brief Title
Periodontal Treatment in Non-controlled Type 2 Diabetes Mellitus Patients. Clinical Trial
Acronym
FONIS12I2106
Official Title
Evaluation of the Effectiveness of Intensive Periodontal Treatment as Compared to Conventional Periodontal Treatment on the Level of Glycosylated Hemoglobin in Patients With Decompensated Type 2 Diabetes Mellitus: Randomized Clinical Trial
Study Type
Interventional

2. Study Status

Record Verification Date
December 2015
Overall Recruitment Status
Completed
Study Start Date
March 2013 (undefined)
Primary Completion Date
December 2015 (Actual)
Study Completion Date
December 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Universidad de los Andes, Chile

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Periodontitis is an infectious disease that destroys the tooth supporting tissues and triggers a local and systemic immune response. Type 2 Diabetes Mellitus (DM2) is a risk factor for periodontitis.Patients with DM2 and periodontitis have greater difficulty getting and maintaining an appropriate glycemic control. It has been reported an average decrease of 0.4% in glycosylated hemoglobin levels (HbA1c) in patients periodontally treated versus untreated. It is not has been established that periodontal treatment type in spaced sessions (multiple sessions over a period of 4 weeks) or rapid and intensive (2 sessions in 24 hours), has a greater impact on glycemic control in type 2 diabetes patients. Objective: To evaluate the effectiveness of intensive periodontal treatment modality as compared with conventional on HbA1c level in periodontitis and DM2 decompensated patients.
Detailed Description
It is proposed to conduct a clinical trial in 100 type 2 diabetic patients with poor glycemic control defined as a glycated hemoglobin (HbA1c) ≥ 7% at last check, with randomization stratified by referral center, with two parallel groups (1: 1). Diabetic patients are in treatment and control in Diabetes Polyclinic Medical Specialty Center of the University of the Andes or the medical polyclinic Joan Alsina in San Bernardo . All decompensated DM2 patients diagnosed with chronic periodontitis will receive periodontal treatment based on 2 different periodontal treatment modalities: the first and most traditional is by spaced sessions by quadrant in 1 weekly session (5 sessions). The second form of treatment corresponds to an intensive periodontal treatment, whole mouth in 24 hours. All patients will be given an initial periodontal examination with manual north carolina periodontal probe, performed by a single operator previously calibrated. Periodontal status will be determine according to the classification of Page and Eke (2007) and periodontal wound size (PISA) will be also determine. Also, will be measured inflammatory mediators and cytokines in both plasma and gingival crevicular fluid (GCF) by ELISA test. The data were entered into a medical record designed specifically for this study and the variables will be recorded prior and at 3 and 6 months after periodontal therapy.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetes Mellitus., Chronic Periodontitis
Keywords
Diabetes mellitus., Periodontitis, Periodontal treatment.

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Investigator
Allocation
Randomized
Enrollment
87 (Actual)

8. Arms, Groups, and Interventions

Arm Title
conventional periodontal treatment
Arm Type
Experimental
Arm Description
Treatment group by quadrant in five weeks. Patients in this group will receive periodontal treatment including plaque control instructions, supragingival and subgingival debridement and root planing. This treatment is done in 5 sessions with a periodicity of 1 session per week. In the first session patients will receive hygiene instruction and supragingival debridement performed with and ultrasonic device. In the following session, there will be done the scaling and root planing to one quadrant per session, using site specific hand curettes. In case of being partially edentulous patients will be implemented at least 3 teeth per quadrant in each session.
Arm Title
Intensive periodontal treatment
Arm Type
Experimental
Arm Description
Intensive treatment group in 24 hours: Patients in this group will receive periodontal treatment including: plaque control instructions, supragingival and subgingival debridement and scaling and root planing. This treatment is carried out in 2 sessions within 24 hours. In the first session hygiene instruction and supragingival and scaling and root planing of the teeth in right side at the upper jaw and mandible will be performed. The implementation of each upper and lower hemiarcade will be made until the periodontist treating check manually the removal of all subgingival calculus deposit and feel the smoothness of the root surface. In the second session, there will be an identical procedure in the arch left.
Intervention Type
Procedure
Intervention Name(s)
conventional periodontal treatment
Other Intervention Name(s)
intensive periodontal treatment
Primary Outcome Measure Information:
Title
Glycated hemoglobin (HbA1c)
Description
Assess levels and relationship of HbA1c in peripheral blood and gingival crevicular fluid at baseline, 3 and 6 months after periodontal treatment in the group of patients treated by intensive and conventional periodontal treatment.
Time Frame
2 years
Secondary Outcome Measure Information:
Title
C-reactive protein
Description
Assess levels and relationship of C-reactive protein, in peripheral blood and gingival crevicular fluid at baseline, 3 and 6 months after periodontal treatment in the group of patients treated by intensive and conventional periodontal treatment .
Time Frame
2 years
Title
Interleukin-6 (IL-6)
Description
Assess levels and relationship of IL-6 in peripheral blood and gingival crevicular fluid at baseline, 3 and 6 months after periodontal treatment in the group of patients treated by intensive and conventional treatment.
Time Frame
2 years
Title
Tumor Necrosis Factor (TNF)
Description
Asses levels and relationship of TNF in peripheral blood and gingival crevicular fluid at baseline, 3 and 6 months after intensive and conventional periodontal treatment.
Time Frame
2 years
Other Pre-specified Outcome Measures:
Title
probing depth
Description
Asses the levels of probing depth baseline, 3 and 6 months after periodontal treatment in the group of patients treated by intensive and conventional treatment.
Time Frame
2 years
Title
gingival bleeding (BOP)
Description
Asses the level of BOP at baseline, 3 and 6 months after periodontal treatment in both groups of patients.
Time Frame
2 years
Title
clinical attachment level (CAL)
Description
Asses the level of CAL baseline, 3 and 6 months after periodontal treatment in the group of patients treated by intensive and conventional treatment.
Time Frame
2 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
30 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Decompensated type 2 diabetic patients (HbA1c ≥ 7% at last check). Minimum 12 teeth in the mouth. no history of surgical or nonsurgical periodontal treatment in the six months prior to baseline. not be involved in another clinical trial. Exclusion Criteria: Patients with renal failure Patients with rheumatoid arthritis, Patients with heart disease. Patients with history of stroke or acute cardiovascular event in the 12 months prior to the start of the study. Patients with liver dysfunction Patients in state of pregnancy or planning pregnancy. Patients on medical treatment with systemic antibiotics in the past 3 months.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Antonio J Quintero, DDS
Organizational Affiliation
Universidad de Los Andes
Official's Role
Principal Investigator
Facility Information:
Facility Name
Joan Alsina Polyclinic
City
San Bernardo
State/Province
Metropolitan
ZIP/Postal Code
8340518
Country
Chile

12. IPD Sharing Statement

Citations:
PubMed Identifier
30024030
Citation
Quintero AJ, Chaparro A, Quirynen M, Ramirez V, Prieto D, Morales H, Prada P, Hernandez M, Sanz A. Effect of two periodontal treatment modalities in patients with uncontrolled type 2 diabetes mellitus: A randomized clinical trial. J Clin Periodontol. 2018 Sep;45(9):1098-1106. doi: 10.1111/jcpe.12991. Epub 2018 Aug 16.
Results Reference
derived

Learn more about this trial

Periodontal Treatment in Non-controlled Type 2 Diabetes Mellitus Patients. Clinical Trial

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