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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05242354
Other study ID # Peri-implant macrophage
Secondary ID
Status Completed
Phase
First received
Last updated
Start date March 1, 2021
Est. completion date December 31, 2021

Study information

Verified date May 2023
Source Biruni University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Macrophage surface markers (CD80, CD163 and CD206) will be evaluated in periodontally healthy gingiva, healthy peri-implant mucosa, and periodontitis and peri-implantitis lesions.


Description:

Soft tissue biopsies obtained from clinically healthy gingiva, healthy peri-implant mucosa, Stage III Grade C periodontitis lesions and peri-implantitis lesions will be evaluated. Healthy peri-implant samples are obtained from submerged implants during exposure surgery. Healthy gingiva samples are obtained from individuals receiving crown lengthening, gingivectomy or tooth extraction as excess tissue during the corresponding treatment. Samples from peri-implantitis and periodontitis (pocket depth ≥6 mm, bleeding on probing+) are obtained during initial periodontal treatment / debridement procedure with a single stroke at the pocket wall. The samples will be grinded and ultrasonicated. Western blotting will be used for determination of CD80, CD163 and CD206 in biopsy specimens. ImageJ will be used for intensity analysis of the bands.


Recruitment information / eligibility

Status Completed
Enrollment 36
Est. completion date December 31, 2021
Est. primary completion date December 31, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - diagnosed with generalized Grade C Stage III periodontitis - diagnosed with peri-implantitis - periodontally healthy individuals with dental implants in the primary healing period - periodontally healthy individuals who are in need of crown lengthening / gingivectomy or extraction Exclusion Criteria: - systemic disease - smoking / former smokers - regular medicine intake - antibiotic or anti-inflammatory medicine intake in the last 3 months - pregnancy or lactation

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Turkey Biruni University Istanbul

Sponsors (2)

Lead Sponsor Collaborator
Biruni University University of Turku

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary CD80 Tissue levels of CD80
Western Blot assay analyzed using Image J software:
Following scanning for optical densitometry, the gels were analyzed with Image J software by obtaining profile plots, drawing lines enclosing the interest area and measuring the peak area of interest with the wand tool. The calculated optical density values are presented as arbitrary density units.
Baseline
Primary CD163 Tissue levels of CD163
Western Blot assay analyzed using Image J software:
Following scanning for optical densitometry, the gels were analyzed with Image J software by obtaining profile plots, drawing lines enclosing the interest area and measuring the peak area of interest with the wand tool. The calculated optical density values are presented as arbitrary density units.
Baseline
Primary CD206 Tissue levels of CD206
Western Blot assay analyzed using Image J software (arbitrary density units):
Following scanning for optical densitometry, the gels were analyzed with Image J software by obtaining profile plots, drawing lines enclosing the interest area and measuring the peak area of interest with the wand tool. The calculated optical density values are presented as arbitrary density units.
Baseline
Primary CD80/CD163 Ratio Tissue levels (Western Blot assay analyzed using Image J software) of CD80 divided by those of CD163 Baseline
Primary CD80/CD206 Ratio Tissue levels (Western Blot assay analyzed using Image J software) of CD80 divided by those of CD206 Baseline
Secondary Probing Depth Probing depth of each site, where the tissue sample was harvested. The average probing depth of sites in each group are presented. Baseline
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