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Oxidative Stress Markers Evaluation Before and After Periodontal Treatment of Diabetics Type 2 Patients

U

University of Sao Paulo

Status and phase

Unknown
Early Phase 1

Conditions

Diabetes Mellitus Type 2

Treatments

Procedure: non- surgical periodontal treatment
Procedure: Prophylaxis

Study type

Interventional

Funder types

Other

Identifiers

NCT01475435
DMSAL2712

Details and patient eligibility

About

Abstract Diabetes mellitus and periodontal diseases are both chronic inflammatory disorders that have a major impact on the health and well being of millions of individuals worldwide. Periodontal diseases are among the most common diseases in humans, therefore, if the presence of periodontal diseases plays any role in overall systemic health, the public health impact may be substantial. An important factor that can be involved in the progression of the periodontal disease is the production of Reactive Oxygen Species (ROS). The imbalance between oxidative stress induced by ROS and the concentrations (or activity) of the antioxidant may result in tissue damage. The ROS induce the activity of lipid peroxidation-Tbars, myeloperoxidase (MPO), peroxidase and arginase, whose mechanisms reflect the severity of the periodontal disease and it may offer the basis for a patient specific diagnostic test for periodontitis and could have therapeutic significance. The aim of this study is to investigate quantitatively the levels of oxidative stress markers (Myeloperoxidase, Peroxidase, Lipid Peroxidation and Arginase) in saliva and in gingival crevicular fluid (GCF) of diabetes type 2 subjects with generalized chronic periodontitis and periodontally healthy individuals, and systematically healthy individuals with generalized chronic periodontitis and periodontally healthy individuals, before and after periodontal treatment. Unstimulated whole saliva will be collected for 5 min as well as GCF of 25 diabetes type 2 with generalized chronic periodontitis, 25 diabetes type 2 periodontally healthy individuals as controls, 25 systematically healthy individuals with generalized chronic periodontitis and 25 periodontally healthy individuals before and after treatment. The following clinical parameters will be evaluated: probing pocket depth, probing attachment level, plaque index and the gingival index. The activity of stress markers in saliva and GFC will be analyzed by spectrophotometry. Adequate statistical analysis will be carried out with a p-value set at p < 0.05.

Enrollment

200 estimated patients

Sex

All

Ages

30 to 70 years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

  • Patients with type 2 diabetes and chronic periodontitis(more than 30% of the sites involved, AAP, 1999)
  • Patients with type 2 diabetes and periodontally healthy (AAP, 1999)
  • Patients systemically healthy with chronic periodontitis (more than 30% of the sites involved)
  • Patients systemically and periodontally healthy
  • Patients with at least 15 natural teeth (excluding 3rd molars).
  • At least 30% of sites with probing pocket depth (PD)> 5 mm and a maximum of 60% sites with PS <7 mm
  • Clinical attachment level (CAL)> 4 mm
  • Visible plaque and bleeding on probing (BOP)
  • Patients with type 2 diabetes have to bear the disease for at least five years and have to show a blood percentage of glycated hemoglobin between 6.5% to 8% (UKPDS 1998) at baseline

Exclusion Criteria

  • Individuals with periodontal pockets deeper than 7 mm
  • Patients with any other systemic disease (except diabetes type 2)
  • Patients who have used medications such as anticoagulants, contraceptives or antidepressants in the past 6 months
  • Patients who have used antibiotic and anti-inflammatory drugs in the last 3 months before the of the study
  • Smoking
  • Pregnancy
  • Patients who have received periodontal treatment in the last six months before the start of this study.

Trial design

Primary purpose

Diagnostic

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

200 participants in 4 patient groups, including a placebo group

chronic periodontitis
Active Comparator group
Description:
Saliva and GCF samples will be evaluated before and after treatment from patients treated of chronic periodontitis.
Treatment:
Procedure: non- surgical periodontal treatment
periodontally healthy individuals
Placebo Comparator group
Description:
Saliva and GCF samples will be evaluated from periodontally healthy individuals at baseline.
Treatment:
Procedure: Prophylaxis
chronic periodontitis with diabetes type 2
Active Comparator group
Description:
Saliva and GCF samples will be evaluated before and after treatment from patients with diabetes type 2 treated of chronic periodontitis
Treatment:
Procedure: non- surgical periodontal treatment
periodontally healthy individuals with diabetes type 2
Placebo Comparator group
Description:
Saliva and GCF samples will be evaluated from periodontally healthy individuals with diabetes type 2 at baseline
Treatment:
Procedure: Prophylaxis

Trial contacts and locations

1

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Central trial contact

Ana Paula Sassá Benedete; Luiz Antônio Pugliesi Alves de Lima, PhD

Data sourced from clinicaltrials.gov

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