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Clinical and Microbiological Evaluation of Periodontal Treatment of Diabetic Patients: A Longitudinal Study

E

Eduardo Aleixo Figueira

Status and phase

Unknown
Phase 2

Conditions

Chronic Periodontitis
Diabetes Mellitus, Type 2

Treatments

Procedure: Full Mouth Scaling and Root Planing

Study type

Interventional

Funder types

Other

Identifiers

NCT02643771
U1111-1175-5481

Details and patient eligibility

About

The purpose of this study is to determine whether periodontal treatment improves the periodontal clinical parameters in the periodontal patients with diabetes regarding non-diabetics: two years follow-up.

Full description

All the subjects in the study will receive non surgical periodontal treatment in one session (full-mouth scaling and root planing). Clinical parameters will be assessed in all teeth (except third molars) by one experienced and trained examiner before treatment and every 3 months for 2 years. Visible plaque index (VPI) will be represented a mean percentage of sites with visible plaque calculated for all teeth analyzed (four sites per tooth). Others parameters will be assessed at six sites per tooth using a manual periodontal probe (15mm). Bleeding on probing (BOP) will be represented the mean percentage of sites with bleeding (up to 15 seconds after probing) calculated for all teeth analyzed. Probing depth (PD - distance between the gingival margin and the bottom of the sulcus/pocket), gingival recession (GR - distance between the cementoenamel junction and gingival margin) and clinical attachment level (CAL - distance between the cementoenamel junction and the bottom of the sulcus/pocket) will be represented a mean distance calculated per site for all teeth analyzed. For blood parameters, an outside laboratory will perform all blood analysis. It will be requested for each subject with diabetes (DG) at baseline, each 3 months post-treatment. Fasting plasma glucose (FPG) will be expressed in milligrams per deciliter and HbA1c will be expressed as a percentage. Statistical analysis will be performed using an available software program and the patient will be considered as the unit of analysis.The data will be processed and analyzed by descriptive and inferential statistics, probably nonparametric.

Enrollment

144 estimated patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Clinical diagnosis of chronical periodontitis according to Lopez et al. 2002 (one or more teeth with at least one site with PD >= 4mm or CAL >= 3mm);
  • And have at least 8 natural teeth (excluding third molars), and older than 18 years and of both genders.

Exclusion criteria

  • Any systemic diseases or complications (except Type 2 Diabetes Mellitus) such as cardiovascular disease, Alzheimer's, lung or brain diseases and metabolic syndrome;
  • Use of antibiotics or periodontal treatment within the past 6 months;
  • Long-term administration of anti-inflammatory or/and immunosuppressive agents;
  • Current smoker or former smoker for the past 5 years;
  • Pregnant or breastfeeding;
  • And presence of orthodontic appliances.

Trial design

Primary purpose

Diagnostic

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

144 participants in 2 patient groups

Diabetic group
Experimental group
Description:
Subjects with Chronic Periodontitis and Type 2 Diabetes Mellitus treated with non surgical periodontal therapy (Full Mouth Scaling and Root Planing)
Treatment:
Procedure: Full Mouth Scaling and Root Planing
Nondiabetic group
Experimental group
Description:
Subjects with Chronic Periodontitis and without Type 2 Diabetes Mellitus treated with non surgical periodontal therapy (Full Mouth Scaling and Root Planing)
Treatment:
Procedure: Full Mouth Scaling and Root Planing

Trial contacts and locations

1

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Central trial contact

Eduardo A Figueira, Doctor; Bruno CV Gurgel, Doctor

Data sourced from clinicaltrials.gov

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