Effects of i-PRF on Non-surgical Periodontal Treatment
Study Details
Study Description
Brief Summary
Injectable platelet-rich fibrin, a platelet concentrate in a liquid formulation, has been developed to provide clinicians with ease of use alone or in combination with various biomaterials. The low-speed centrifugation method provides a significant advantage to the regeneration process with richer platelets, leukocytes, and growth factors. It also contributes to the wound-healing process by increasing vascularization. It is expected that the application of injectable platelet-rich fibrin into the gingival pocket following subgingival curettage in periodontitis patients will positively affect the results of non-surgical periodontal treatment. For this reason, in this study it was aimed to investigate the early effects of injectable PRF applied into the pocket for root surface biomodification following subgingival curettage in periodontal pockets of 6 mm and above, by evaluating both clinical parameters and inflammatory and healing markers in the gingival groove fluid
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
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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 Design
Arms and Interventions
| Arm | 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. |
Procedure: non surgical periodontal treatment
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:
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| SRP (Control) No agent was applied to the periodontal pocket after scaling and root planning. |
Procedure: non surgical periodontal treatment
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:
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Outcome Measures
Primary Outcome Measures
- GCF VEGF levels in test and control groups [Change from Baseline GCF VEGF levels at 3rd and 7th days]
measure and compare the improvement of VEGF in test and control groups by using ELISA
- GCF TNF-alpha levels in test and control groups [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
- GCF IL-10 levels in test and control groups [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
- Plaque index (PI) [Change from Baseline PI at 3rd and 7th days]
measure and compare the improvement of PI in test and control groups using a scale
- Probing depth (PD) [Change from Baseline PD levels at 3rd and 7th days]
measure the gingival margin to pocket bottom as mm and compare the improvement of PD in test and control groups
- Gingival index (GI) [Change from Baseline GI at 3rd and 7th days]
measure and compare the improvement of GI in test and control groups using a scale
- Bleeding on probing (BOP) [Change from Baseline BOP at 3rd and 7th days]
Whether there is bleeding when the periodontal pocket is probed and comparing the improvement in test and control groups
- Clinical attachment level (CAL) [Change from Baseline CAL at 3rd and 7th days]
measure the distance from the cemento-enamel line to the bottom of the pocket and compare the improvement in test and control groups
Eligibility Criteria
Criteria
Inclusion Criteria:
- patients with stage 3 grade B periodontitis
Exclusion Criteria:
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patients with systemic disease
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pregnant and breastfeeding
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acute or chronic infection in the past 6 months
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Use of systemic antibiotic therapy in the past 6 months
-
use of drugs that can affect periodontal health
-
receiving hormone therapy
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smokers
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teeth with endodontic lesions
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Teeth with class 2 and 3 mobility
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Gizem Torumtay Cin | Denizli | Deni̇zli̇ | Turkey | 20070 |
Sponsors and Collaborators
- Pamukkale University
Investigators
- Principal Investigator: Gizem Torumtay Cin, PhD, pamukkale university faculty of dentistry
Study Documents (Full-Text)
None provided.More Information
Publications
- 22.02.2022/04