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Clinical Trials/NCT02190409
NCT02190409
Completed
Not Applicable

The Effect Of Platelet Rich Fibrin on Implant Stability

ELİF ONCU1 site in 1 country20 target enrollmentDecember 2011
ConditionsDental Implant

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Dental Implant
Sponsor
ELİF ONCU
Enrollment
20
Locations
1
Primary Endpoint
Implant Stabilitty Quotient (ISQ) evaluation: analysis of the resonance frequency values 4 week period.
Status
Completed
Last Updated
11 years ago

Overview

Brief Summary

The purpose of this study was to evaluate the effects of (Platelet Rich Fibrin) PRF application on implant osseointegration in the early phase of healing.

Detailed Description

Objectives:Achieving accelerated implant osseointegration could provide immediate or early loading of implants. Platelet-rich fibrin (PRF) is widely used to accelerate soft and hard tissue healing. Activated platelets in PRF release growth factors resulting in cellular proliferation, collagen synthesis and osteoid production. The aim of this study was to compare the stability of dental implants inserted with one-stage surgical protocol with or without PRF application. Design: Non-randomized, Active Controlled Trial. Material and Methods: Twenty healthy patients (n=10 test group, n= control group) with adequate alveolar bone, having 2 or more adjacent missing teeth, extracted at least 6 months ago were included in this study. Minimum two tapered implants (Ankylosis, DentsplyFriadent) were placed to each patient. After surgical preparation of implant sockets, PRF that was prepared preoperatively was placed randomly to one of the sockets (PRF+). Acellular plasma portion of PRF was used to wet the implant placed into the PRF-coated socket. Resonance frequency measurements were made by Osstell ISQ after placement of implants, at 1 week and one month postoperatively. Key Words: Dental implant stability, Platelet Rich Fibrin, Resonance frequency analysis

Registry
clinicaltrials.gov
Start Date
December 2011
End Date
December 2012
Last Updated
11 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
ELİF ONCU
Responsible Party
Sponsor Investigator
Principal Investigator

ELİF ONCU

Assist.Prof.Dr.

Necmettin Erbakan University

Eligibility Criteria

Inclusion Criteria

  • The absence of any lesions in the oral cavity, and sufficient residual bone volume to receive two or more adjacent implants of ≥3.5 mm in diameter and 11.0 mm in length, and extracted at least 6 months ago.

Exclusion Criteria

  • Insufficient bone volume
  • Parafunctional habits
  • Smoking more than 10 cigarettes per day
  • Excessive consumption of alcohol
  • Localized radiotherapy of the oral cavity
  • Antitumor chemotherapy
  • Liver, blood, and kidney diseases
  • Immunosuppression
  • Current corticosteroid or bisphosphonate use
  • Pregnancy

Outcomes

Primary Outcomes

Implant Stabilitty Quotient (ISQ) evaluation: analysis of the resonance frequency values 4 week period.

Time Frame: Resonance frequency measurements were made by Osstell ISQ after placement of implants, at 1 week and one month postoperatively.

The stability of the implants were evaluated with the resonance frequency analysis (RFA) method. The measurements were carried out with Osstell ISQ (Implant Stability Quotient) (Osstell, Göteborg, Sweden) by connecting the transducer (smartpeg) to the implant. Two mesio-distal and bucco-lingual measurements were recorded and mean ISQ values were calculated. The resonance frequency measurements were repeated at first and fourth weeks.

Secondary Outcomes

  • Evaluation of osseointegration in different types of bone(Resonance frequency measurements in different bone types were made by Osstell ISQ after placement of implants, at 1 week and one month postoperatively.)

Study Sites (1)

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