NCT07596667

Brief Summary

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).

Trial Health

65
Monitor

Trial Health Score

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

Enrollment
21

participants targeted

Target at below P25 for not_applicable

Timeline
5mo left

Started Jul 2026

Shorter than P25 for not_applicable

Status
not yet recruiting

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

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

May 7, 2026

Completed
12 days until next milestone

First Posted

Study publicly available on registry

May 19, 2026

Completed
2 months until next milestone

Study Start

First participant enrolled

July 15, 2026

Expected
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 15, 2026

16 days until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2026

Last Updated

May 19, 2026

Status Verified

May 1, 2026

Enrollment Period

4 months

First QC Date

May 7, 2026

Last Update Submit

May 18, 2026

Conditions

Keywords

periodontitisnon surgical periodontal therapy

Outcome Measures

Primary Outcomes (3)

  • periodontal pocket depth

    periodontal pocket depth reduction

    3 months

  • measurement of probing pocket depth (PPD)

    measuring probing pocket depth (PPD)

    3 months

  • measurement of clinical attachment loss (CAL)

    clinical attachment loss (CAL)

    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

    3 months

Study Arms (1)

periodontitis patients with pocket depth

EXPERIMENTAL
Procedure: scaling and root planing

Interventions

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).

periodontitis patients with pocket depth

Eligibility Criteria

Age18 Years - 60 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • patients over 18 years old
  • patients with periodontal pockets depth more than 4 mm

You may not qualify if:

  • Pregnant women
  • patients taking antibiotic within the last three months
  • Patients with systemic disease ( Diabetes mellitus)

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Related Publications (1)

  • Vitkov L, Singh J, Schauer C, Minnich B, Krunic J, Oberthaler H, Gamsjaeger S, Herrmann M, Knopf J, Hannig M. Breaking the Gingival Barrier in Periodontitis. Int J Mol Sci. 2023 Feb 25;24(5):4544. doi: 10.3390/ijms24054544.

    PMID: 36901974BACKGROUND

MeSH Terms

Conditions

Chronic PeriodontitisPeriodontal DiseasesPeriodontitis

Interventions

Tooth ExfoliationRoot Planing

Condition Hierarchy (Ancestors)

Mouth DiseasesStomatognathic DiseasesChronic DiseaseDisease AttributesPathologic ProcessesPathological Conditions, Signs and Symptoms

Intervention Hierarchy (Ancestors)

Dental Physiological PhenomenaDigestive System and Oral Physiological PhenomenaDental ScalingDental ProphylaxisPeriodonticsDentistrySubgingival CurettagePreventive Dentistry

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
TREATMENT
Intervention Model
SINGLE GROUP
Model Details: Periodontitis patients (n = 21) will be included in this clinical trial. Clinical periodontal parameters will be recorded and GCF samples will be 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).
Sponsor Type
OTHER
Responsible Party
SPONSOR INVESTIGATOR
PI Title
Assistant Professor

Study Record Dates

First Submitted

May 7, 2026

First Posted

May 19, 2026

Study Start (Estimated)

July 15, 2026

Primary Completion (Estimated)

November 15, 2026

Study Completion (Estimated)

December 1, 2026

Last Updated

May 19, 2026

Record last verified: 2026-05