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Evaluation of GCF And Salivary Ferritin, ALP And MMP-8 Levels of Individuals With Different Periodontal Diseases

I

Izmir Katip Celebi University

Status

Completed

Conditions

Periodontal Diseases

Treatments

Diagnostic Test: GCF and saliva obtaining

Study type

Interventional

Funder types

Other

Identifiers

NCT06561802
2019-TDR-SABE-0009

Details and patient eligibility

About

The aim of this clinical study was to determine the levels of ferritin, alkaline phosphatase and matrix metalloproteinase-8 in the gingival crevicular fluid (GCF) and saliva samples were collected from 60 systemically healthy, non-smoker periodontitis (P group, n = 20), gingivitis (G group, n = 20) and periodontally healthy individuals (S group, n = 20) and all clinical parameters were recorded for all groups at baseline. GCF and serum samplings and clinical records were also repeated at 1st and 3rd months visitsfor only P group. Ferritin, MMP8, and ALP levels in samples were determined by enzyme-linked immunosorbent assay (ELISA).

Enrollment

60 patients

Sex

All

Ages

18 to 60 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Systemically healthy

  • At least twenty permanent teeth in the mouth

  • Non-smoker

  • No medication for continuous use

  • Those who have not used antibiotics, anti-inflammatory and systemic corticosteroid drugs in the last 6 months.

  • Not in pregnancy or lactation period.

  • For the periodontitis group that has not received periodontal treatment in the last 6 months

    • For the periodontitis group; According to the evaluation made in 6 regions of each tooth, individuals with 30% or more bleeding on probing area, at least 2 teeth not adjacent to each quarter jaw with a depth of 5 mm or more and 4 mm or more attachment loss, coronal 1/3 and more on radiography (horizontal and / or vertical) bone loss
    • For the gingivitis group; According to the evaluation made in 6 regions of each tooth, individuals with 10% or more bleeding on probing area, having a probing depth of less than 4mm and no attachment loss
    • For healthy group; According to the evaluation made in 6 regions of each tooth,individuals with less than 10% bleeding on probing area, having a probing depth less than 4mm and no loss of attachment were included in the study.

Exclusion criteria

  • Any oral or systemic disease
  • Regularly using a systemic medication
  • During pregnancy or lactation
  • Received periodontal treatment within the last 6 months.
  • Those who received antibiotic, anti-inflammatory or systemic corticosteroid medication in the last 6 months
  • Smokers are not included in the study

Trial design

Primary purpose

Diagnostic

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

60 participants in 3 patient groups

periodontally healthy
Experimental group
Description:
Full-mouth clinical periodontal measurements recorded and GCF and saliva obtained.
Treatment:
Diagnostic Test: GCF and saliva obtaining
gingivitis
Experimental group
Description:
Full-mouth clinical periodontal measurements recorded and GCF and saliva obtained.
Treatment:
Diagnostic Test: GCF and saliva obtaining
periodontitis
Experimental group
Description:
Full-mouth clinical periodontal measurements recorded and GCF and saliva obtained.
Treatment:
Diagnostic Test: GCF and saliva obtaining

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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