Effects of i-PRF on Non-surgical Periodontal Treatment

February 22, 2023 updated by: AYSAN LEKTEMUR ALPAN, Pamukkale University

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

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

Study Overview

Status

Completed

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

Observational

Enrollment (Actual)

24

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Deni̇zli̇
      • Denizli, Deni̇zli̇, Turkey, 20070
        • Gizem Torumtay Cin

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 65 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Patients with systemically healthy and stage 3 grade B periodontitis aged 18-65

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

This section provides details of the study plan, including how the study is designed and what the study is measuring.

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:
  • i-PRF application
  • clinical periodontal measurement taken
  • gingival crevicular fluid obtained
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:
  • i-PRF application
  • clinical periodontal measurement taken
  • gingival crevicular fluid obtained

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
measure and compare the improvement of VEGF in test and control groups by using ELISA
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
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
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
measure and compare the improvement of PI in test and control groups using a scale
Change from Baseline PI at 3rd and 7th days
Probing depth (PD)
Time Frame: 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
Change from Baseline PD levels at 3rd and 7th days
Gingival index (GI)
Time Frame: Change from Baseline GI at 3rd and 7th days
measure and compare the improvement of GI in test and control groups using a scale
Change from Baseline GI at 3rd and 7th days
Bleeding on probing (BOP)
Time Frame: 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
Change from Baseline BOP at 3rd and 7th days
Clinical attachment level (CAL)
Time Frame: 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
Change from Baseline CAL at 3rd and 7th days

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Gizem Torumtay Cin, PhD, Pamukkale University Faculty of Dentistry

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

February 2, 2022

Primary Completion (Actual)

November 15, 2022

Study Completion (Actual)

January 15, 2023

Study Registration Dates

First Submitted

January 18, 2023

First Submitted That Met QC Criteria

February 22, 2023

First Posted (Estimate)

March 3, 2023

Study Record Updates

Last Update Posted (Estimate)

March 3, 2023

Last Update Submitted That Met QC Criteria

February 22, 2023

Last Verified

February 1, 2023

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

IPD Plan Description

It is planned to be given if requested with a valid reason.

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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