Non Surgical Periodontal Treatment Effect on Il-17 and Il-18 in Aggressive Periodontitis

Aggressive Periodontitis Clinical Trial

Official title:

Effect of Non Surgical Periodontal Treatment on Clinical Parameters and Gingival Crevicular Fluid Il-17 and Il-18 Levels in Aggressive Periodontitis Patients

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT05297084
• Other study ID #: FUE11
• Status: Completed
• 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
• 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.

Related Conditions & MeSH terms

• Aggression
• Aggressive Periodontitis
• Periodontitis

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