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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT06291454
Other study ID # 741100
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 1, 2023
Est. completion date December 1, 2023

Study information

Verified date March 2024
Source T.C. ORDU ÜNIVERSITESI
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

This study aimed to determine CCL19/MIP3beta(β) and CCL20/MIP3alpha(α) in the gingival crevicular fluid (GCF) of the patients with different periodontitis phenotypes. A total of 72 individuals, 24 with Stage III Grade B periodontitis (Group 1), 24 with Stage III Grade C periodontitis (Group 2), and 24 periodontally healthy (control group) (Group 3), were included in the study. GCF and clinical periodontal parameters were obtained at baseline. MIP3β and MIP3α levels in GCF were determined by ELISA.


Recruitment information / eligibility

Status Completed
Enrollment 72
Est. completion date December 1, 2023
Est. primary completion date December 1, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 22 Years to 55 Years
Eligibility Inclusion Criteria: - Have at least 20 natural teeth, excluding third molars. - Periodontitis patients had at least two non-adjacent sites per quadrant with probing depth (PD) = 5 mm and clinical attachment level (CAL) = 5 mm with gingival inflammation, and alveolar bone loss affecting >30% of the teeth, as detected on clinical and radiographical examinations. - Periodontally healthy control group had no sign of gingival inflammation, no PD > 3mm and no evidence of attachment or bone loss Exclusion Criteria: - History of systemic disease. - Regular use of any drugs which can effect the immune system or inflammatory response in the 6 months preceding the start of the study. - Periodontal treatment during last 6 months that could affect periodontal status. - Smoking. - History of radiotherapy or chemotherapy. - Current pregnancy, lactation or menopause.

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
Routine periodontal examination
In all of the patients, the following indexes were used routinely for the periodontal examination: Sillness-Löe's plaque index (PI) (Silness & Löe, 1964), Löe-Sillness's gingival index (GI)(Löe & Silness, 1963), probing depth (PD) to measure the extent and severity of periodontal disease, clinical attachment level (CAL), and bleeding on probing (BOP)(Ainamo & Bay, 1975) to determine activity. In addition, routine radiographic evaluations were performed to determine bone levels.GCF samples were collected using standardized filter papers.

Locations

Country Name City State
Turkey Ordu University, Faculty of Dentistry Ordu

Sponsors (1)

Lead Sponsor Collaborator
T.C. ORDU ÜNIVERSITESI

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary CCL19/MIP3beta(ß) levels CCL19/MIP3beta(ß) levels in the gingival crevicular fluid (GCF) of the all groups Baseline
Primary CCL20/MIP3alpha(a) levels CCL20/MIP3alpha(a) levels in the gingival crevicular fluid (GCF) Baseline
Secondary CCL19/MIP3beta(ß) levels and clinical parameters Correlation between CCL19/MIP3beta(ß) levels in the gingival crevicular fluid (GCF) of the all groups and all clinical parameters Baseline
Secondary CCL20/MIP3alpha(a) levels and clinical parameters Correlation between CCL20/MIP3alpha(a) levels in the gingival crevicular fluid (GCF) of the all groups and all clinical parameters Baseline
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