NCT05297084

Brief 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 .

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
50

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Mar 2021

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

March 27, 2021

Completed
9 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 15, 2021

Completed
15 days until next milestone

Study Completion

Last participant's last visit for all outcomes

December 30, 2021

Completed
2 months until next milestone

First Submitted

Initial submission to the registry

March 2, 2022

Completed
23 days until next milestone

First Posted

Study publicly available on registry

March 25, 2022

Completed
Last Updated

April 7, 2022

Status Verified

March 1, 2022

Enrollment Period

9 months

First QC Date

March 2, 2022

Last Update Submit

March 30, 2022

Conditions

Keywords

gingival crevicular fluid

Outcome Measures

Primary Outcomes (1)

  • 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

Study Arms (2)

Aggressive periodontitis

25 young medically free patients with deep periodontal pockets \>5mm

Procedure: non surgical periodontal therapy

Periodontally healthy individuals

25 young medically free individuals with no periodontal inflammation signs

Interventions

Scaling and root planing

Aggressive periodontitis

Eligibility Criteria

Age18 Years - 30 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)
Sampling MethodNon-Probability Sample
Study Population

Both genders Age between 18 and 30 years old

You may qualify if:

  • Medically free subjects.

You may not qualify if:

  • 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.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Faculty of oral and dental medicine,FUE, Cairo,Egypt

Cairo, 11835, Egypt

Location

Biospecimen

Retention: SAMPLES WITHOUT DNA

Periopaper strips stored in Eppendorf tubes

MeSH Terms

Conditions

Aggressive Periodontitis

Condition Hierarchy (Ancestors)

PeriodontitisPeriodontal DiseasesMouth DiseasesStomatognathic Diseases

Study Officials

  • Sarah M Elkot, Lecturer

    Lecturer of Oral Medicine and Periodontology

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Lecturer of Oral Medicine, Periodontology and Diagnosis, Faculty of Oral and Dental Medicine, Future University in Egypt, Cairo, Egypt.

Study Record Dates

First Submitted

March 2, 2022

First Posted

March 25, 2022

Study Start

March 27, 2021

Primary Completion

December 15, 2021

Study Completion

December 30, 2021

Last Updated

April 7, 2022

Record last verified: 2022-03

Locations