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The Effect of Non-Surgical Periodontal Treatment on Bone Metabolism in Type 2 Diabetes and Systemically Healthy Individuals

N

Necmettin Erbakan University

Status

Completed

Conditions

Periodontal Diseases

Treatments

Diagnostic Test: ELISA

Study type

Interventional

Funder types

Other

Identifiers

NCT05862311
Ummuhantekinatay.

Details and patient eligibility

About

In this study, it was concluded that sclerostin and irisin may be alternative markers for evaluating the effectiveness of periodontal treatment and healing of periodontal tissues by affecting bone metabolism.

Full description

Background: Diabetes and periodontitis are chronic inflammatory diseases with similar pathogenesis and clinical and immunological interrelationships. The aim of this study is to determine periodontal clinical parameters and sclerostin, irisin, Receptor Activator of Nuclear Factor κB Ligand (RANKL)/Osteoprotegerin (OPG), interleukin-6 (IL-6) and tumor necrosis factor-α (TNF-α) levels in gingival crevicular fluid (GCF) in individuals with type 2 diabetes and systemically healthy periodontitis and to evaluate the effect of non-surgical periodontal therapy on these clinical parameters and biomarkers.

Method: Within the scope of this study, applying to Necmettin Erbakan University Faculty of Dentistry Periodontology Clinic; A total of 50 individuals, including 25 patients with type 2 diabetes and periodontitis (DMP group) and 25 patients with systemically healthy and periodontitis (SSP group), were included in the study. After recording the clinical periodontal parameters (gingival index (GI), plaque index (PI), probing pocket depth (PPD), clinical attachment level (CAL)) of each individual included in the study, GCF samples were obtained and non-surgical periodontal therapy were completed. The individuals were invited to the controls 3 months later and the procedures for clinical periodontal measurements and DOS samples collection were repeated. Levels of biomarkers in DOS samples were determined by ELISA (Enzyme Linked Immunosorbent Assay) method.

Enrollment

50 patients

Sex

All

Ages

18 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Having at least 20 teeth in the mouth, excluding the third molars,
  • Individuals between the ages of 18-65
  • Diagnosed as stage 2 or stage 3 periodontitis as a result of periodontal examination
  • Those who do not have predisposing factors (restoration, caries, etc.)

Exclusion criteria

  • Smoking or using alcohol,
  • Any periodontal treatment performed in the last 6 months,
  • Being in pregnancy and/or lactation period,
  • Individuals who had received any anti-inflammatory, antibiotic, antioxidant or corticosteroid treatment in the last 6 months and refused to participate in the study were excluded from the study.

Trial design

Primary purpose

Diagnostic

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

50 participants in 2 patient groups

systemically healthy and periodontitis
Experimental group
Treatment:
Diagnostic Test: ELISA
type 2 diabetes and periodontitis
Experimental group
Treatment:
Diagnostic Test: ELISA

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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