- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05753631
Effects of i-PRF on Non-surgical Periodontal Treatment
Evaluation of the Effects of Injectable Platelet-rich Fibrin (i-PRF) Application on Periodontal Clinical and Biochemical Parameters in Gingival Crevicular Fluid (GCF) in Non-surgical Periodontal Treatment
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The study was planned as a randomized controlled split-mouth clinical trial. A split-mouth design was used to better assess how the same host responded to two different treatment modalities. Two quadrants with contralateral deep periodontal pockets in each participant were selected and randomly divided into test and control groups.
Test group: Injectable platelet-rich fibrin application into the selected deep periodontal pocket after scaling and root planning (SRP) procedure.
Control group: No agent was applied to the periodontal pocket after scaling and root planning.
On the first visit, clinical periodontal measurements were taken before the SRP procedure. Plague index (PI), gingival index (GI), probing depth (PD), clinical attachment level (CAL), and bleeding on probing (BOP) were used as clinical periodontal parameters.
After 1 week, the patients were called again for the SRP procedure. Injectable PRF obtained from the intravenous blood sample taken from the antecubital vein of the patients was injected into the deepened periodontal pocket subgingivally after the SRP procedure in the test group. Clinical periodontal measurements at 1 month and 3 months after SRP were repeated.
Gingival crevicular fluid (GCF) samples were taken from selected teeth before the SRP procedure. On the 3rd and 7th day after the SRP, GCF samples were taken again from the same region.
GCF vascular endothelial growth factor (VEGF), tumor necrosis factor-alpha (TNF-α), and interleukin (IL)-10 levels were evaluated by using the ELISA method and compared between groups.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Deni̇zli̇
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Denizli, Deni̇zli̇, Turkey, 20070
- Gizem Torumtay Cin
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- patients with stage 3 grade B periodontitis
Exclusion Criteria:
- patients with systemic disease
- pregnant and breastfeeding
- acute or chronic infection in the past 6 months
- Use of systemic antibiotic therapy in the past 6 months
- use of drugs that can affect periodontal health
- receiving hormone therapy
- smokers
- teeth with endodontic lesions
- Teeth with class 2 and 3 mobility
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
SRP+i-PRF (test)
Injectable platelet-rich fibrin (i-PRF) application into the selected deep periodontal pocket after scaling and root planning (SRP) procedure.
|
scaling and root planning were applied for non-surgical periodontal treatment i-PRF application: Intravenous blood sample taken from the antecubital vein of the patients was collected in a 10 ml tube and centrifuged at 700 rpm for 3 minutes in a PRF centrifuge device. The PRF obtained from the upper liquid layer formed in the tube was injected subgingival into the deepest point of the pocket after SRP treatment. Clinical periodontal measurements: plaque index, gingival index, probing depth, clinical attachment level, bleeding on probing, and gingival recession were calculated. gingival crevicular fluid: Perio papers were placed in the deepest part of the sulcus and left for 30 seconds. After 30 seconds, the paper strips were placed in the periotron device and the volume was calculated.
Other Names:
|
|
SRP (Control)
No agent was applied to the periodontal pocket after scaling and root planning.
|
scaling and root planning were applied for non-surgical periodontal treatment i-PRF application: Intravenous blood sample taken from the antecubital vein of the patients was collected in a 10 ml tube and centrifuged at 700 rpm for 3 minutes in a PRF centrifuge device. The PRF obtained from the upper liquid layer formed in the tube was injected subgingival into the deepest point of the pocket after SRP treatment. Clinical periodontal measurements: plaque index, gingival index, probing depth, clinical attachment level, bleeding on probing, and gingival recession were calculated. gingival crevicular fluid: Perio papers were placed in the deepest part of the sulcus and left for 30 seconds. After 30 seconds, the paper strips were placed in the periotron device and the volume was calculated.
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
GCF VEGF levels in test and control groups
Time Frame: Change from Baseline GCF VEGF levels at 3rd and 7th days
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measure and compare the improvement of VEGF in test and control groups by using ELISA
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Change from Baseline GCF VEGF levels at 3rd and 7th days
|
|
GCF TNF-alpha levels in test and control groups
Time Frame: Change from Baseline GCF TNF-alpha levels at 3rd and 7th days
|
measure and compare the improvement of TNF-alpha in test and control groups by using ELISA
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Change from Baseline GCF TNF-alpha levels at 3rd and 7th days
|
|
GCF IL-10 levels in test and control groups
Time Frame: Change from Baseline GCF IL-10 levels at 3rd and 7th days
|
measure and compare the improvement of IL-10 in test and control groups by using ELISA
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Change from Baseline GCF IL-10 levels at 3rd and 7th days
|
|
Plaque index (PI)
Time Frame: Change from Baseline PI at 3rd and 7th days
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measure and compare the improvement of PI in test and control groups using a scale
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Change from Baseline PI at 3rd and 7th days
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Probing depth (PD)
Time Frame: Change from Baseline PD levels at 3rd and 7th days
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measure the gingival margin to pocket bottom as mm and compare the improvement of PD in test and control groups
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Change from Baseline PD levels at 3rd and 7th days
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|
Gingival index (GI)
Time Frame: Change from Baseline GI at 3rd and 7th days
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measure and compare the improvement of GI in test and control groups using a scale
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Change from Baseline GI at 3rd and 7th days
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Bleeding on probing (BOP)
Time Frame: Change from Baseline BOP at 3rd and 7th days
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Whether there is bleeding when the periodontal pocket is probed and comparing the improvement in test and control groups
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Change from Baseline BOP at 3rd and 7th days
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Clinical attachment level (CAL)
Time Frame: Change from Baseline CAL at 3rd and 7th days
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measure the distance from the cemento-enamel line to the bottom of the pocket and compare the improvement in test and control groups
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Change from Baseline CAL at 3rd and 7th days
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Gizem Torumtay Cin, PhD, Pamukkale University Faculty of Dentistry
Publications and helpful links
General Publications
- Miron RJ, Fujioka-Kobayashi M, Hernandez M, Kandalam U, Zhang Y, Ghanaati S, Choukroun J. Injectable platelet rich fibrin (i-PRF): opportunities in regenerative dentistry? Clin Oral Investig. 2017 Nov;21(8):2619-2627. doi: 10.1007/s00784-017-2063-9. Epub 2017 Feb 2.
- Choukroun J, Diss A, Simonpieri A, Girard MO, Schoeffler C, Dohan SL, Dohan AJ, Mouhyi J, Dohan DM. Platelet-rich fibrin (PRF): a second-generation platelet concentrate. Part IV: clinical effects on tissue healing. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2006 Mar;101(3):e56-60. doi: 10.1016/j.tripleo.2005.07.011.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 22.02.2022/04
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
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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