Effect of Non Surgical Periodontal Therapy on Inflammatory Markers in Chronic Periodontitis Patients

Sponsor
Future University in Egypt (Other)
Overall Status
Completed
CT.gov ID
NCT05295576
Collaborator
(none)
50
1
9.1
5.5

Study Details

Study Description

Brief Summary

The current study was performed to study levels of Il-17 and Il-18 in aggressive periodontitis patients before and after non surgical periodontal therapy

Condition or Disease Intervention/Treatment Phase
  • Procedure: non surgical periodontal therapy

Detailed Description

Background:host defense factors are involved in pathogenesis of chronic periodontitis so, the current study is assessing levels of Il-17 and Il-18 in chronic periodontitis patients versus periodontally healthy controls.

Subjects and methods: Fifty subjects were included; twenty five of them are diagnosed with chronic periodontitis patients and twenty five are periodontally healthy subjects. Probing depth (PD), clinical attachment level (CAL), plaque index (PI) and gingival index (GI) were recorded for all the enrolled subjects. GCF levels of Il-17 and IL-18 were analyzed by enzyme-linked immunosorbent assay (ELISA).

Study Design

Study Type:
Observational
Actual Enrollment :
50 participants
Observational Model:
Case-Control
Time Perspective:
Prospective
Official Title:
Effect of Non Surgical Periodontal Therapy on Levels of Il-17 and Il-18 in Chronic Periodontitis Patients Versus Periodontally Healthy Individuals
Actual Study Start Date :
Mar 27, 2021
Actual Primary Completion Date :
Dec 15, 2021
Actual Study Completion Date :
Dec 30, 2021

Arms and Interventions

Arm Intervention/Treatment
chronic periodontitis

scaling and root planing

Procedure: non surgical periodontal therapy
Scaling and root planing

Periodontally healthy individuals

no treatment

Outcome Measures

Primary Outcome Measures

  1. measure levels of Il-17 and Il-18 in chronic periodontitis patients [Change from Baseline Il-17 andIl-18 at 3 months]

    measure levels of Il-17 and Il-18 in GCF of chronic periodontitis patients

Eligibility Criteria

Criteria

Ages Eligible for Study:
30 Years to 60 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Medically free subjects .

  • both genders .

  • age range between 30 to 60 years old .

Exclusion Criteria:
  • Subjects with periodontal surgeries in the last 6 months.

  • Subjects with prior use of antibiotics in the last 6 months.

  • Smokers.

  • Pregnant and lactating females were excluded.

  • Lactating females.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Future university in Egypt Cairo Egypt 11835

Sponsors and Collaborators

  • Future University in Egypt

Investigators

  • Principal Investigator: Sarah M Elkot, Lecturer, Lecturer of Oral Medicine and Periodontology

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Sarah Elkot, Lecturer of Oral Medicine, Periodontology and Diagnosis, Faculty of Oral and Dental Medicine, Future University in Egypt, Cairo, Egypt., Future University in Egypt
ClinicalTrials.gov Identifier:
NCT05295576
Other Study ID Numbers:
  • FUE12
First Posted:
Mar 25, 2022
Last Update Posted:
Mar 25, 2022
Last Verified:
Mar 1, 2022
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 25, 2022