- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05994885
Evaluation of Prognostic Potentials of Gingival Crevicular Fluid E-cadherin and Total Antioxidant Capacity
Prognostic Potentials of E-cadherin and Total Antioxidant Capacity in Gingival Crevicular Fluid of Moderately Deep Periodontal Pockets Treated With Nonsurgical Periodontal Therapy
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Loss of attachment and formation of periodontal pockets are hallmarks of periodontitis. The treatment approach is either by nonsurgical or surgical periodontal therapy or a combination of both depending on the severity of the case. In general, sites with moderately deep pockets (4 to 6 mm) are responding favorably to nonsurgical periodontal therapy (NSPT). Nevertheless, some sites exhibit persistent pockets even with multiple treatment sessions which could be attributed to the presence of tissue invaders or aberrant immune response that impede healing process.
Prediction of treatment outcomes based on clinical data is limited and sometimes lacking accuracy. Use of biomarkers that can be non-invasively collected from oral fluids e.g., gingival crevicular fluid (GCF) as diagnostic/predictive tools has gained attention in the last decade. For instance, E-Cadherin (E-cad) and total antioxidant capacity (TAC) are associated with periodontitis. E-cad is a transmembrane glycoprotein that is a key mediator of stable cell-cell adhesion of epithelial cells. E-cadherin-based adherens junctions specialized cell structures that mediate cell-cell adhesion and regulate cytoskeleton reorganization forming a continuous, linear circumferential belt (zonula adherens) around the apical part of the cell. While TAC, defined as the moles of oxidants neutralized by one liter of solution, is a biomarker measuring the antioxidant potential of body fluids.
Available evidence indicates that the concentration of both molecules are substantially increased with increasing severity of periodontitis and vice versa in periodontal health. This suggests the potential of GCF-E-cad and TAC to predict the prognosis following NSPT.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Ali A Abdulkareem, PhD
- Phone Number: 07806866717
- Email: ali.abbas@codental.uobaghdad.edu.iq
Study Locations
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Baghdad, Iraq
- Recruiting
- College of Dentistry/ University of Baghdad
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Contact:
- Ali A Abdulkareem, PhD
- Phone Number: 009647806866717
- Email: ali.abbas@codental.uobaghdad.edu.iq
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Systemically healthy adult patients (> 18 years).
- Periodontitis (interdental clinical attachment loss (CAL) detectable at ≥2 non-adjacent teeth, or buccal/oral CAL of ≥3mm with pocketing of >3mm is detectable at ≥2 teeth). All patients should exhibit generalized periodontitis with pockets of PPD = 4 to 6 mm of any stage, unstable, and grade A to C. Only maxillary teeth with single root will be included.
Exclusion Criteria:
- Consumption of antibiotics or periodontal treatment 3-months prior to the study.
- Pregnancy and lactation.
- Smoker.
- History of systemic disease e.g., diabetes mellitus.
- Patients currently recruited in other trials.
- Patients not willing to consent.
- Periodontal pockets ≥ 7mm, active caries, endodontic problem.
- Multi-rooted teeth will be also considered as exclusion reasons.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Other: Root surface debridement
Periodontal pockets with PPD of 4 to 6mm are treated with root surface debridement only and assessed after 3 months for success/failure of treatment.
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the included patients will undergo full-mouth supra- and subgingival debridement by using ultrasonic device and manual instrumentation at baseline.
This is followed, after 1 week, by performing root surface debridement for all pockets with PPD = 4-6 mm for each patient.
All patients will be instructed to brush their teeth twice daily and will be supplied with the same type of tooth paste and toothbrush, with suitable interdental aids.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Probing pocket depth
Time Frame: Baseline, 1 week, then 1 month and 3 months after treatment
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Linear distance, in mm, measured from the gingival margin to the base of periodontal pocket or sulcus.
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Baseline, 1 week, then 1 month and 3 months after treatment
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Clinical attachment loss
Time Frame: Baseline, 1 week, then 1 month and 3 months after treatment
|
Linear distance, in mm, measured from the cementoenamel junction to the base of periodontal pocket or sulcus.
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Baseline, 1 week, then 1 month and 3 months after treatment
|
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Bleeding on probing
Time Frame: Baseline, 1 week, then 1 month and 3 months after treatment
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Presence or absence of bleeding is detected after 30 seconds of inserting periodontal probe to the depth of periodontal pocket/sulcus
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Baseline, 1 week, then 1 month and 3 months after treatment
|
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Gingival crevicular fluid E-cadherin
Time Frame: Baseline, 1 month and 3 months after treatment
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Level of E-cadherin in GCF collected from periodontal pockets is determined by biochemical analysis
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Baseline, 1 month and 3 months after treatment
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Total antioxidant capacity
Time Frame: Baseline, 1 month and 3 months after treatment
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Level of TAC in GCF collected from periodontal pockets is determined by biochemical analysis
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Baseline, 1 month and 3 months after treatment
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Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 747622
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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