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CompletedNCT07695857Updated Jul 10, 2026

Adropin Levels in Periodontal Disease

An observational study in Periodontitis, sponsored by Giresun University. Completed at 1 site in Turkey (Türkiye). Open to participants aged 27 Years to 49 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-07-10.

Sponsored by Giresun University · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
60
Ages
27 Years to 49 Years
Sex
All
01

Study summary

This study aimed to evaluate gingival crevicular fluid (GCF) and serum levels of Adropin and tumor necrosis factor (TNF)-alfa in patients with periodontitis before and after non-surgical periodontal therapy.

Read the detailed description

Thirty periodontitis and thirty periodontally healthy individuals were enrolled in the study. Clinical periodontal measurements were recorded; periodontitis patients received non-surgical periodontal treatment, and GCF and serum samples were collected at baseline and at 6 weeks after treatment. Adropin and TNF-alfa were determined by ELISA.

02

Conditions studied

  • Periodontitis

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Keywords

  • periodontitis
  • Adropin
  • gingival crevicular fluid
  • serum
03

In context

Periodontitis

1,635 studies on the registry are indexed under Periodontitis; 327 are open to participants now.

This study's enrollment of 60 is below the median of 90 across 428 observational studies indexed under Periodontitis.

Browse Periodontitis studies →

Lead sponsor

Giresun University is the lead sponsor of 51 studies on the registry; 4 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
27 Years to 49 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Criteria for healthy control group: BOP \< 10% and PD ≤ 3 mm without clinical attachment loss or radiographic sign of alveolar bone destruction.

Criteria for periodontitis group: interdental CAL ≥ 5 mm at least 2 non-adjacent teeth, PD ≥ 6 mm and radiographic bone loss extending to the mid-third of the root or beyond.

Inclusion criteria

  • having at least 20 natural teeth, excluding third molars
  • having no systemic disease
  • non-smokers
  • Diagnosed with periodontally health and periodontitis patients

Exclusion criteria

Exclusion Criteria:

  • having any systemic diseases
  • smoking
  • current pregnancy or lactation
  • a history of periodontal treatment in the past 6 months
  • using antibiotic, anti-inflammatory drugs or any other drugs within the past 6 months.
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
60 participants (actual)
Patient registry
No
Biospecimen retention
Samples without dna

Groups and cohorts

  • Group 1: Periodontally healthy individuals
  • Group 2: Periodontitis patients

    Procedure: Nonsurgical periodontal therapy

Interventions

  • ProcedureNonsurgical periodontal therapy

    Nonsurgical periodontal therapy includes oral hygiene education and scaling and root planning approaches to eliminate microbial dental biofilm that is the primary etiology of periodontal diseases.

06

What researchers measure

Primary outcomes

  1. 1. Adropin levels

    Changes in Adropin levels before and after periodontal therapy

    Time frame: Baseline and at 6 weeks after therapy

Secondary outcomes

  1. TNF-alfa levels

    Changes in TNF-alfa levels before and after periodontal therapy

    Time frame: baseline and at 6 weeks after therapy

07

Study locations

1 site
  • Giresun University
    Giresun, Turkey (Türkiye)
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 10, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT07695857
Lead sponsor
Giresun University
Collaborators
Aydin Adnan Menderes University
Responsible party
Zeynep Pınar Yucel (Assoc. Prof., DDS, PhD, Giresun University) — Principal investigator
First posted
Jul 10, 2026
Start date
Apr 2, 2018
Primary completion
Sep 2, 2020
Completion
Nov 6, 2020
Last update
Jul 10, 2026

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jan 2026. You cannot join it, but the record below documents what was studied.

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