PRF Growth Factors Levels in Diabetic Patients With Chronic Periodontitis
NCT ID: NCT02304497
Last Updated: 2014-12-02
Study Results
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Basic Information
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COMPLETED
80 participants
OBSERVATIONAL
2013-03-31
2014-11-30
Brief Summary
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Detailed Description
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This study consisted of 80 subjects; 20 patients were T2DM with periodontally healthy (DM-CTRL), 20 patients were T2DM with chronic periodontitis (DM-CP ), 20 patients were systemically healthy with chronic periodontitis (CP; ), 20 subjects were systemically and periodontally healthy (CTRL).
Subjects were clinically evaluated with regards to the plaque index (PI), gingival index (GI), probing pockets depth (PD), clinical attachment level (CAL), bleeding on probing (BOP) recorded at six sites per tooth (disto-facial, mid-facial, mesio-facial, mesio-lingual, disto-lingual and mid-lingual) using a periodontal Goldman/Fox Williams probe calibrated in millimeters.
PRF was prepared without biochemical manipulation of blood. Intravenous blood from each patient was collected in 10 ml sterile tubes without anticoagulant by venipuncture of antecubital vein. Immediately test tubes were centrifuged using a centrifugation machine ( Electro.mag M 815 P Laboratory Centrifuge ; Istanbul, Turkey) at 2700 rpm ( approximately 700g ) for 12 min . The centrifuged blood presented with a structured fibrin clot in the middle of the tube just between the red corpuscles at the bottom and acellular plasma at the top. PRF was easily separated from the red corpuscule base using steril scissors and inserted into steril tubes. The tubes were put on a shaker and agitated gently. After 5 minutes, the tubes were vortexed to form a PRF membrane and the volume of releasate was measured and the releasate returned into the tube. The tubes were further agitated gently. Samples were taken at 5th minute and immediately centrifuged at 5000rpm for 15 minutes (Electro.mag M 815 P Laboratory Centrifuge ; Istanbul, Turkey) to pellet any residual blood cells , and were stored at -80 centigrade degree for subsequent assays.
Samples were assayed by using enzyme-linked immunosorbent assay (ELISA) with an ELX 800 G ELISA device (BIO-TEC Instruments, Winooski, USA). The following ELISA kits were used in this study: b-FGF, TGF-β2 and IGF 1 (Assay Biotechnology Company, CA, USA); PDGF-AB, VEGF and TGF-β1 (Boster Biological Technology, CA, USA).
Statistical analysis was performed using a commercially available software (SPSS 15.0; SPSS Inc., Chicago, IL). The Shapiro-Wilk test was used to investigate whether the data were normally distributed. When normal distribution with equal variances was assumed in PDGF-AB, VEGF, TGF-β1, variables were compared using one-way analysis of variance (ANOVA) with Bonferroni post hoc test. If the assumption of normality failed, comparisons of the age, TGF-β2, b-FGF, IGF-1, HbA1c, fasting blood glucose, postprandial blood glucose, full-mouth PD, CAL, GI, PI and BOP were tested using the Kruskal-Wallis non-parametric test followed by post-hoc group comparisons with the Bonferroni-adjusted Mann-Whitney U test.
Conditions
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Study Design
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CASE_CONTROL
PROSPECTIVE
Study Groups
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DM-CTRL
Diabetes mellitus patients with periodontally healthy Platelet Rich Fibrin obtained
Platelet Rich Fibrin
Procedure: Platelet Rich Fibrin obtained
DM-CP
Diabetes mellitus patients with chronic periodontitis Platelet Rich Fibrin obtained
Platelet Rich Fibrin
Procedure: Platelet Rich Fibrin obtained
CP
Chronic periodontitis patients with systemically healthy Platelet Rich Fibrin obtained
Platelet Rich Fibrin
Procedure: Platelet Rich Fibrin obtained
CTRL
Periodontally and systemically healthy subject Platelet Rich Fibrin obtained
Platelet Rich Fibrin
Procedure: Platelet Rich Fibrin obtained
Interventions
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Platelet Rich Fibrin
Procedure: Platelet Rich Fibrin obtained
Eligibility Criteria
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Inclusion Criteria
* No periodontal treatment in the prior 6 months.
* T2DM patients who had HbA1c levels between 6%-8 %
* Periodontally healthy subjects (periodontal pocket depth \< 4 mm)
Exclusion Criteria
* Patient had been under medicine treatment for at least 6 months except patients with diabetes who were treated with stable doses of hypoglycemic agents
* Patients with major complications of DM (i.e., cardiovascular and peripheral vascular diseases
* Insufficient platelet count (\<200,000/mm3); 2) pregnancy/lactation )
* Tobacco use
* Pregnancy
40 Years
65 Years
ALL
Yes
Sponsors
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Bulent Ecevit University
OTHER
Responsible Party
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Seyma Bozkurt Doğan
PhD, DDS
Principal Investigators
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Şeyma Bozkurt Doğan, DDS
Role: STUDY_CHAIR
Bülent Ecevit University Faculty of Dentistry
Umut Ballı, DDS
Role: PRINCIPAL_INVESTIGATOR
Bülent Ecevit University Faculty of Dentistry
Figen Öngöz Dede, DDS
Role: STUDY_DIRECTOR
Bülent Ecevit University Faculty of Dentistry
Mustafa Cenk Durmuşlar, DDS
Role: PRINCIPAL_INVESTIGATOR
Bülent Ecevit University Faculty of Dentistry
Murat Can, Assoc. Professor
Role: PRINCIPAL_INVESTIGATOR
Bülent Ecevit University Faculty of Medicine
Other Identifiers
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2013-62550515-01
Identifier Type: -
Identifier Source: org_study_id