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 volunteersQualifiers
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
Single group
Treatments tested in this trial
scaling and root planing
Procedure/SurgeryPeriodontitis 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
Trial outcomes
Primary outcomes
periodontal pocket depth
periodontal pocket depth reduction
measurement of probing pocket depth (PPD)
measuring probing pocket depth (PPD)
measurement of clinical attachment loss (CAL)
clinical attachment loss (CAL)
Secondary outcomes
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
Locations
Sponsors and contacts
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