Gingival Crevicular Fluid Vaspin and Omentin Levels in Type 2 Diabetic Patients With Chronic Periodontitis
NCT ID: NCT02544347
Last Updated: 2015-11-03
Study Results
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Basic Information
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COMPLETED
NA
60 participants
INTERVENTIONAL
2014-07-31
2015-06-30
Brief Summary
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Detailed Description
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A total of 15 T2DM patients with CP ( DM-CP group), 15 CP patients (CP group), 15 T2DM patients (DM-CTRL group) and 15 subjects with systemically and periodontally healthy control subjects (CTRL group) were included in the study. Diabetic subjects should have T2DM and had no any known systemic diseases other than T2DM. The glycemic status of patients previously diagnosed with T2DM was confirmed by their glycated haemoglobin (HbA1c) levels. Periodontal disease status was determined according to clinical and radiographic criteria by the 1999 classification of periodontal disease.
Subjects were clinically evaluated using the following parameters; plaque index (PI), gingival index (GI) , PD, clinical attachment level (CAL) and BOP (deemed positive if it occurred within 15 seconds after probing). Clinical measurements were recorded by one calibrated examiner at six sites per tooth from the full-mouth teeth excluding third molars using with a Williams periodontal probe (Nordent Manufacturing Inc., ElkGrove Village, IL, USA) calibrated in millimeters. Anthropometric measurements included weight (kg) and height (m) of the subjects to calculate the BMI ( weight divided by the square of height, kg/m2 ).
All clinical and radiological examinations, sampling site selections were performed by one examiner and the samples were collected on the day after clinical examination of patients. This was to prevent contamination of GCF with blood associated with the probing of inflamed sites. The deepest two pocket sites of single-rooted teeth were selected for the collection of GCF in both periodontitis groups, and also two pocket sites with an absence of inflammation were sampled to ensure the collection of an adequate amount of GCF in control groups. In patients from CP and DM-CP groups, sites showing greatest PD when measured with a periodontal probes and signs of inflammation, along with radiographic conformation of bone loss were sampled. GCF samples were collected at baseline and after 8 weeks from baseline sampling in both periodontitis groups, and only at baseline in control groups. To avoid salivary contamination, the sites to be sampled were rinsed with water, isolated by cotton rolls and gently air dried. Paper strips (Periopaper; Oraflow Inc.,Smithtown, NY, USA) were gently inserted 1-2 mm into the sulcus/pocket for 30 seconds. Care was taken to avoid mechanical injury of the gingival tissues. All samples containing blood and saliva were discarded. The two strips from two sites of each individual were placed into coded sealed plastic eppendorf tubes and pooled before freezing at -80 degree
Conditions
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Study Design
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NON_RANDOMIZED
SINGLE_GROUP
TREATMENT
SINGLE
Study Groups
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diabetes mellitus group
gingival crevicular fluid was collected
gingival crevicular fluid
gingival crevicular fluid was collected
Control group
gingival crevicular fluid was collected
gingival crevicular fluid
gingival crevicular fluid was collected
diabetics with chronic periodontitis group
non-surgical periodontal treatment was completed and gingival crevicular fluid was collected
gingival crevicular fluid
gingival crevicular fluid was collected
non-surgical periodontal treatment
scaling and root planing were performed
chronic periodontitis group
non-surgical periodontal treatment was completed and gingival crevicular fluid was collected
gingival crevicular fluid
gingival crevicular fluid was collected
non-surgical periodontal treatment
scaling and root planing were performed
Interventions
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gingival crevicular fluid
gingival crevicular fluid was collected
non-surgical periodontal treatment
scaling and root planing were performed
Eligibility Criteria
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Inclusion Criteria
* Subjects who had HbA1c levels \< 8% and ≥ 6.5% (well and moderate control)
* Chronic periodontitis patients had radiographic evidence of bone loss and attachment loss with a minimum of 6 teeth having pocket probing depth (PD) ≥ 5mm in at least 2 different quadrants
* Control groups were designed as healthy if the full-mouth probing depth (PD) was ≤3mm and bleeding on probing (BOP) score \< %15 at examination and they had no radiographic evidence of alveolar bone loss.
Exclusion Criteria
* Administration of non-steroidal and anti-inflammatory drugs or antibiotic therapies within the previous 6 months;
* Need for antibiotic prophylaxis for dental treatment and having received non-surgical periodontal treatment within the past 6 months or surgical periodontal treatment within the past 12 months.
* Subjects who had body mass index (BMI) \>24.9 kg /m2
35 Years
65 Years
ALL
Yes
Sponsors
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Bulent Ecevit University
OTHER
Responsible Party
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Seyma Bozkurt Doğan
Asisstant Proffessor, Bulent Ecevit University
Principal Investigators
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Umut Ballı, DDS
Role: PRINCIPAL_INVESTIGATOR
Bülent Ecevit University Faculty of Dentistry
Şeyma Bozkurt Doğan, DDS
Role: STUDY_CHAIR
Bülent Ecevit University Faculty of Dentistry
Figen Öngöz Dede, DDS
Role: PRINCIPAL_INVESTIGATOR
Bülent Ecevit University Faculty of Dentistry
Erdim Sertoğlu, MD, DDS
Role: PRINCIPAL_INVESTIGATOR
Gülhane Military Medical Academy
Other Identifiers
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2014-116-17/06
Identifier Type: -
Identifier Source: org_study_id
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