Profiling Gingival Crevicular Fluid β-Catenin Level With 8-OHdG and Total Antioxidants Capacity During Healing of Periodontal Pockets: A 3-month Clinical Trial

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-60
SponsorZeyad Nazar

About this trial

Background: To profile gingival crevicular fluid (GCF) β-Catenin, 8-OHdG, and total antioxidants capacity (TAC) in periodontitis patients during healing of periodontal pockets following non-surgical periodontal therapy (NSPT).Methods: Periodontitis patients (n = 21) will included in this clinical trial. Clinical periodontal parameters will recorded and GCF samples will collected from randomly selected 4-6 mm periodontal pockets at baseline (T0) as well as 4 weeks (T1) and 12 weeks (T2) after NSPT. GCF levels of β-catenin, 8-OHdG, and TAC will be assayed by enzyme linked immunosorbent assay (ELISA).

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

patients over 18 years old

patients with periodontal pockets depth more than 4 mm

Disqualifiers

Pregnant women

patients taking antibiotic within the last three months

Patients with systemic disease ( Diabetes mellitus)

Trial design

Design model

Single group

Treatments tested in this trial

  • scaling and root planing

    Procedure/Surgery

    Periodontitis patients (n = 21) will included in this clinical trial. Clinical periodontal parameters will recorded and GCF samples will collected from randomly selected 4-6 mm periodontal pockets at baseline (T0) as well as 4 weeks (T1) and 12 weeks (T2) after NSPT. GCF levels of β-catenin, 8-OHdG, and TAC will be assayed by enzyme linked immunosorbent assay (ELISA).

Treatment groups

21 Participants
are divided into 1 treatment group
Group A: periodontitis patients with pocket depthExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

periodontal pocket depth

periodontal pocket depth reduction

Time frame
3 months
2

measurement of probing pocket depth (PPD)

measuring probing pocket depth (PPD)

Time frame
3 months
3

measurement of clinical attachment loss (CAL)

clinical attachment loss (CAL)

Time frame
3 months

Secondary outcomes

1

GCF levels of β-catenin, 8-OHdG, and TAC will be assayed by enzyme linked immunosorbent assay (ELISA) in which all have the same measuring units

GCF levels of β-catenin, 8-OHdG, and TAC will be assayed by enzyme linked immunosorbent assay (ELISA) after 3 months

Time frame
3 months

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Zeyad Nazar

Lead sponsor

Babylon University

Sponsor institution

Babylon University

Collaborator

This trial is not recruiting at the moment. You can still explore other options: