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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05297084
Other study ID # FUE11
Secondary ID
Status Completed
Phase
First received
Last updated
Start date March 27, 2021
Est. completion date December 30, 2021

Study information

Verified date March 2022
Source Future University in Egypt
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

clinical parameters and IL-17 and Il-18 GCF levels were measured in 25 aggressive periodontitis patients compared to 25 periodontally healthy individuals. It was observed that that Clinical parameters and Il-17 and Il-18 levels are higher before treatment but decreased after treatment which suggests role of these interleukins in pathogenesis of aggressive periodontitis .


Description:

Aggressive periodontitis is a type of rapidly progressing periodontal diseases .The three classic primary characteristics of this disease are ; occurring in young healthy patients with rapid attachment loss and familial aggregation .Bacteria-host interactions, insufficiencies in host defenses and possibly a genetic predisposition represent the etiologic factors . Beside the young age of onset, important factors as involvement of host factors and non-plaque-related etiologic factors have also been proposed . Aim of the study: Objectives were to compare and correlate the clinical parameters and biochemical parameters (Il-17 and Il-18 levels in GCF) of aggressive periodontitis patients (At baseline and after three months of nonsurgical treatment) versus periodontally healthy subjects at baseline. Subjects and methods: Populations included in the study: A total of fifty individuals were enrolled and categorized as; group A that included twenty five aggressive periodontitis patients and group B which included twenty five periodontally healthy controls. Clinical parameters: Plaque index (PI) ,gingival index (GI), Probing pocket depth (PPD) and clinical attachment level (CAL) were measured at baseline for both groups and after three months of non surgical periodontal treatment completion for group A. GCF sampling: In group A ,the site with deepest probing depth was selected for GCF sampling while for group B , any site was sampled using PerioPaper strips . Phase I periodontal treatment After baseline GCF sample collection and clinical measurement recordings, group A patients received phase I periodontal treatment. Analysis of Il-17 and Il-18 levels in GCF: GCF samples were examined by enzyme-linked immunosorbent assay (ELISA).Procedures were performed according to the directions in the kits.


Recruitment information / eligibility

Status Completed
Enrollment 50
Est. completion date December 30, 2021
Est. primary completion date December 15, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 30 Years
Eligibility Inclusion Criteria: -Medically free subjects. Exclusion Criteria: - Subjects with periodontal surgeries in the last 6 months. - Subjects with prior use of antibiotics in the last 6 months. - Smokers. - Pregnant females. - Lactating females.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
non surgical periodontal therapy
Scaling and root planing

Locations

Country Name City State
Egypt Faculty of oral and dental medicine,FUE, Cairo,Egypt Cairo

Sponsors (1)

Lead Sponsor Collaborator
Future University in Egypt

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Periopaper strips Il-17 and Il-18 GCF measurements measurement of Il-17 and Il-18 in GCF from aggressive periodontitis patients using periopaper strips Change from Baseline Il-17 and Il-18 at 3 months
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