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Netrin 1 and Its Receptor Unc5b as Markers of Periodontal Disease

Primary Purpose

Periodontitis

Status
Completed
Phase
Not Applicable
Locations
Turkey
Study Type
Interventional
Intervention
non surgical periodontal treatment
Gingival crevicular fluid, saliva and serum collection
Sponsored by
Abant Izzet Baysal University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Periodontitis focused on measuring periodontal diseases, cytokines, gingival crevicular fluid, saliva, serum

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Aged >18 years,
  • Having at least 16 natural teeth (excluding third molar),
  • Nonsmokers with no history of smoking,
  • Not having any diagnosed medical illness or drug intake that could affect the periodontal condition.

Exclusion Criteria:

  • Patients who had taken antibiotics, nonsteroidal antiinflammatory or any other drugs within the past 3 months,
  • Patients received nonsurgical or surgical periodontal treatment,
  • Patients who have a restorative and endodontic therapy requirement,
  • Having a removable partial denture and/or having orthodontic therapy,
  • Current pregnancy or lactation and having serum CRP > 3mg/L .

Sites / Locations

  • Bolu Abant Izzet Baysal University

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Active Comparator

Placebo Comparator

Arm Label

Periodontitis

Gingivitis

Periodontally healthy

Arm Description

GCF, saliva and serum samples were taken before and after treatment from periodontitis patients. Intervention: Non- surgical periodontal treatment (SRP and oral hygiene instructions)

GCF, saliva and serum samples were taken before and after treatment from gingivitis patients. Intervention: Non- surgical periodontal treatment (Scaling and oral hygiene instructions)

GCF, saliva and serum samples were taken at baseline from periodontally healthy individuals.

Outcomes

Primary Outcome Measures

Biochemical parameters (Netrin-1 and Unc5b)
The changes in levels of Netrin-1 and Unc5b 4 weeks after periodontal treatment determined by ELISA. The changes in levels of Netrin-1 and Unc5b were analyzed to determine as a diagnostic biomarker of periodontal disease.

Secondary Outcome Measures

Probing pocket depth
The changes in probing pocket depth was measured for determining severity of disease and clinical outcome
Clinical attachment loss
The changes in probing pocket depth was measured for determining severity of disease
Gingival index
Gingival index was recorded for classifying and evaluating sulcular gingival inflammation. Gingival index was also analyzed to detect the relationship between Netrin-1 and Unc5b.
Plaque index
Plaque index was recorded for determining and classifying oral hygiene status
Bleeding on probing
Bleeding on probing was recorded for classifying and evaluating gingival inflammation especially for apically sulcular inflammation. This was also analyzed to detect the relationship between Netrin-1 and Unc5b.
Papillar bleeding index
Papillar bleeding index was recorded for classifying and evaluating the papillar gingival inflammation. This index was also analyzed to detect the relationship between Netrin-1 and Unc5b.

Full Information

First Posted
April 15, 2019
Last Updated
April 17, 2019
Sponsor
Abant Izzet Baysal University
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1. Study Identification

Unique Protocol Identification Number
NCT03919006
Brief Title
Netrin 1 and Its Receptor Unc5b as Markers of Periodontal Disease
Official Title
Levels of Netrin 1 and Its Receptor Unc5b in Gingival Crevicular Fluid, Saliva and Serum in Periodontal Disease and Health
Study Type
Interventional

2. Study Status

Record Verification Date
April 2019
Overall Recruitment Status
Completed
Study Start Date
January 1, 2018 (Actual)
Primary Completion Date
February 1, 2019 (Actual)
Study Completion Date
April 1, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Abant Izzet Baysal University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
This study aimed to investigate gingival crevicular fluid (GCF), saliva and serum Netrin 1 and Unc5b levels in periodontal health and disease. A total of 60 individuals, 20 patients with periodontitis, 20 with gingivitis and 20 periodontally healthy individuals were included. Whole-mouth and site-specific clinical periodontal parameters including probing depth, clinical attachment level, bleeding on probing, gingival index, plaque index and papillar bleeding index were recorded. GCF, salivary and serum Netrin 1 and Unc5b levels were measured by enzyme-linked immunosorbent assay. Statistical analysis was performed by using non-parametric tests.
Detailed Description
A total of 60 individuals, comprising 20 patients with Periodontitis (P Group), 20 patients with gingivitis (G Group), and 20 periodontally healthy controls (H Group) were involved in the study. The patients were diagnosed according to the new classification scheme. Stage and extent of periodontitis were also determined. The clinical periodontal criteria for the diagnosis of the groups were as follows: the periodontitis group had interdental clinical attachment loss (CAL) ≥5 mm at site of greatest loss and periodontal probing depth (PD) ≥ 6 mm in one or more sites of the 2 non-adjacent teeth in at least two quadrants of the mouth. Accordingly, Stage III generalized periodontitis patients were included in the study. Patients were diagnosed as gingivitis with bleeding on probing ≥ 50 %, PD ≤3 mm, and no radiographic bone loss or CAL. Periodontally healthy individuals had no recorded history of periodontal problems, with PD ≤3 mm, no radiographic bone loss, good oral hygiene, no gingival inflammation. Inclusion criteria were as follows: (1) aged >18 years, (2) having at least 16 natural teeth (excluding third molar),(3) nonsmokers with no history of smoking, (4) not having any diagnosed medical illness or drug intake that could affect the periodontal condition. The patients who had (1) taken antibiotics, nonsteroidal antiinflammatory or any other drugs within the past 3 months,(2) received nonsurgical or surgical periodontal treatment, (3) a restorative and endodontic therapy requirement, (4) a removable partial denture and/or having orthodontic therapy were excluded from the study. Current pregnancy or lactation and having serum C reactive protein (CRP) > 3mg/L were also the exclusion criteria. All individuals were examined at baseline and four weeks after non-surgical periodontal treatment including, whole mouth probing depth (PD), CAL, presence of bleeding on probing (BOP), papillar bleeding index (PBI), gingival index (GI) and plaque index (PI) except the third molars. PD and CAL were measured at six sites per tooth using a manual periodontal probe. The non-surgical periodontal treatment for periodontitis group included supra- and subgingival scaling, root planing and oral hygiene instructions. Subgingival scaling and root planing were performed under local anesthesia in two sessions within the 48-72 h. Gingivitis group had supra-and subgingival scaling, polishing and oral hygiene instructions. The treatment of gingivitis and periodontitis patients were performed by a periodontist (BM) using hand and ultrasonic instruments. All measurements were performed by the same calibrated examiner (SG). Saliva sampling Whole unstimulated saliva samples were collected. Each participant was asked first to rinse the mouth completely with tap water for 1 minutes, wait for 10 minutes, and then expectorate into sterile polypropylene tube for 5 minutes. Gingival crevicular fluid (GCF) sampling GCF samples were obtained from two nonadjacent interproximal sites in one single- rooted and one multi-rooted teeth by standardized filter paper strips. GCF was sampled from two sites with GI < 1, PD ≤ 3 mm and without BOP in the healthy group; two sites with GI ≥ 2, PD ≤ 3 mm and positive BOP (visible signs of inflammation) in the gingivitis group; and two deepest pocket (≥ 5 mm) with GI ≥ 2 and positive BOP in periodontitis group. Serum sampling Serum samples were taken following saliva and GCF sampling before the periodontal treatment. Six milliliters of venous blood were obtained by a standard venipuncture method and the serum was separated from blood by centrifugation at 1,500 g for 20 minutes. Measurement of Netrin 1 and Unc5b levels in GCF, Saliva and Serum Samples Netrin 1 and Unc5b levels in GCF, saliva and serum samples were measured by the enzyme-linked immunosorbent assay (ELISA) using commercial kits according to the manufacturer's guidelines. Statistical Analysis All data analyses were performed using a statistical software package. Comparisons of clinical and biochemical parameters between the study groups were performed using the Kruskal- Wallis with Mann Whitney U test with Bonferroni correction method. The intragroup comparisons (at baseline and first month) were performed using Wilcoxon test for paired samples. Associations among levels of the GCF, saliva and serum biomarkers and clinical parameters were also examined using the Spearman rank correlation analysis.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Periodontitis
Keywords
periodontal diseases, cytokines, gingival crevicular fluid, saliva, serum

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Parallel Assignment
Masking
Outcomes Assessor
Masking Description
Single (Outcomes Assessor)
Allocation
Non-Randomized
Enrollment
60 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Periodontitis
Arm Type
Active Comparator
Arm Description
GCF, saliva and serum samples were taken before and after treatment from periodontitis patients. Intervention: Non- surgical periodontal treatment (SRP and oral hygiene instructions)
Arm Title
Gingivitis
Arm Type
Active Comparator
Arm Description
GCF, saliva and serum samples were taken before and after treatment from gingivitis patients. Intervention: Non- surgical periodontal treatment (Scaling and oral hygiene instructions)
Arm Title
Periodontally healthy
Arm Type
Placebo Comparator
Arm Description
GCF, saliva and serum samples were taken at baseline from periodontally healthy individuals.
Intervention Type
Other
Intervention Name(s)
non surgical periodontal treatment
Intervention Description
SRP under local anaesthesia, in a total of 2 clinical visits. Oral hygiene instructions including the modified Bass technique and an appropriate interdental cleaning device with dental floss and interdental brush.
Intervention Type
Other
Intervention Name(s)
Gingival crevicular fluid, saliva and serum collection
Intervention Description
GCF with filter paper using the intracrevicular method, saliva and serum collection
Primary Outcome Measure Information:
Title
Biochemical parameters (Netrin-1 and Unc5b)
Description
The changes in levels of Netrin-1 and Unc5b 4 weeks after periodontal treatment determined by ELISA. The changes in levels of Netrin-1 and Unc5b were analyzed to determine as a diagnostic biomarker of periodontal disease.
Time Frame
Baseline and 4 weeks after treatment
Secondary Outcome Measure Information:
Title
Probing pocket depth
Description
The changes in probing pocket depth was measured for determining severity of disease and clinical outcome
Time Frame
Baseline and 4 weeks after treatment
Title
Clinical attachment loss
Description
The changes in probing pocket depth was measured for determining severity of disease
Time Frame
Baseline and 4 weeks after treatment
Title
Gingival index
Description
Gingival index was recorded for classifying and evaluating sulcular gingival inflammation. Gingival index was also analyzed to detect the relationship between Netrin-1 and Unc5b.
Time Frame
Baseline and 4 weeks after treatment
Title
Plaque index
Description
Plaque index was recorded for determining and classifying oral hygiene status
Time Frame
Baseline and 4 weeks after treatment
Title
Bleeding on probing
Description
Bleeding on probing was recorded for classifying and evaluating gingival inflammation especially for apically sulcular inflammation. This was also analyzed to detect the relationship between Netrin-1 and Unc5b.
Time Frame
Baseline and 4 weeks after treatment
Title
Papillar bleeding index
Description
Papillar bleeding index was recorded for classifying and evaluating the papillar gingival inflammation. This index was also analyzed to detect the relationship between Netrin-1 and Unc5b.
Time Frame
Baseline and 4 weeks after treatment

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Aged >18 years, Having at least 16 natural teeth (excluding third molar), Nonsmokers with no history of smoking, Not having any diagnosed medical illness or drug intake that could affect the periodontal condition. Exclusion Criteria: Patients who had taken antibiotics, nonsteroidal antiinflammatory or any other drugs within the past 3 months, Patients received nonsurgical or surgical periodontal treatment, Patients who have a restorative and endodontic therapy requirement, Having a removable partial denture and/or having orthodontic therapy, Current pregnancy or lactation and having serum CRP > 3mg/L .
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sadiye Gunpinar, Asst. Prof.
Organizational Affiliation
Abant Izzet Baysal University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Bolu Abant Izzet Baysal University
City
Bolu
ZIP/Postal Code
14030
Country
Turkey

12. IPD Sharing Statement

Citations:
PubMed Identifier
29926951
Citation
Papapanou PN, Sanz M, Buduneli N, Dietrich T, Feres M, Fine DH, Flemmig TF, Garcia R, Giannobile WV, Graziani F, Greenwell H, Herrera D, Kao RT, Kebschull M, Kinane DF, Kirkwood KL, Kocher T, Kornman KS, Kumar PS, Loos BG, Machtei E, Meng H, Mombelli A, Needleman I, Offenbacher S, Seymour GJ, Teles R, Tonetti MS. Periodontitis: Consensus report of workgroup 2 of the 2017 World Workshop on the Classification of Periodontal and Peri-Implant Diseases and Conditions. J Periodontol. 2018 Jun;89 Suppl 1:S173-S182. doi: 10.1002/JPER.17-0721.
Results Reference
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PubMed Identifier
29926489
Citation
Caton JG, Armitage G, Berglundh T, Chapple ILC, Jepsen S, Kornman KS, Mealey BL, Papapanou PN, Sanz M, Tonetti MS. A new classification scheme for periodontal and peri-implant diseases and conditions - Introduction and key changes from the 1999 classification. J Clin Periodontol. 2018 Jun;45 Suppl 20:S1-S8. doi: 10.1111/jcpe.12935.
Results Reference
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Netrin 1 and Its Receptor Unc5b as Markers of Periodontal Disease

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