The Clinical and Biological Effects of Leucocyte and Platelet-rich Fibrin (L-PRF) on Post-extraction Sockets Healing

NCT ID: NCT03985033

Last Updated: 2022-01-11

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

18 participants

Study Classification

INTERVENTIONAL

Study Start Date

2019-10-01

Study Completion Date

2021-12-31

Brief Summary

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This study evaluates the clinical and biological effects of leucocyte and platelet-rich fibrin (L-PRF) on post-extraction sockets healing.

Detailed Description

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Tooth extraction is one of the most frequent dental surgical procedures. Following tooth extraction, dimensional changes of the alveolus are inevitable, which consequently decrease the height and width of alveolar bone and impair ideal implant placement and conventional prosthetic treatment. In order to reduce the bone resorption after tooth extraction, the use of platelet concentrates has been proposed. Platelet rich fibrin (PRF) is a second generation of platelet concentrates consisting of platelets, leukocyte and growth factors harvested from blood. PRF not only supports hemostasis but also favors the natural wound healing process. Over the past decade, PRF has gained tremendous momentum having been utilized for a variety of dental and medical procedures including the management of post-extraction sockets. To date, several studies have assessed the efficacy of the use of PRF in promoting postextraction sockets healing. However, results remain contradictory and mainly focus on the clinical and radiological hard and soft tissue healing, aesthetics and postoperative discomfort. The mechanistic hypothesis is that growth factors released by PRF preparations modulate the wound healing process but the effect of local PRF application on the kinetics of release of wound healing modulators has not been studied so far. There is also a lack of information in the literature regarding the biological evaluation during postextraction sockets healing to understand the potential mechanisms. In order to assess the presence or follow dynamics of biomarkers, in this study wound fluid (WF) will be collected from the post-extraction sockets and utilized for multiplex immunoassay. Multiplex immunoassay allows simultaneous quantification of multiple markers providing unique information for a more complete understanding of the potential mechanism of PRF and spontaneous extraction socket healing. Therefore, the aim of this randomized clinical trial is to evaluate the effects of PRF on biomarkers response during post-extraction sockets healing.

Conditions

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Tooth Extraction

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Split-mouth design allowing to assess two types of treatment in the same patient.
Primary Study Purpose

BASIC_SCIENCE

Blinding Strategy

DOUBLE

Caregivers Outcome Assessors

Study Groups

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L-PRF

Post-extraction sockets will be filled with autologous leucocyte and platelet-rich fibrin (L-PRF) clot.

Group Type EXPERIMENTAL

leucocyte and platelet-rich fibrin (L-PRF)

Intervention Type OTHER

The blood collected from each patient will be centrifuged immediately at 2700 rpm for 12 min to separate L-PRF.

Control

Post-extraction sockets will be left to heal spontaneously with natural blood clot.

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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leucocyte and platelet-rich fibrin (L-PRF)

The blood collected from each patient will be centrifuged immediately at 2700 rpm for 12 min to separate L-PRF.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Participant is willing and able to give informed consent for participation in the study
* Healthy males and females of age 18-70
* Need for two or more extractions of single rooted teeth in the presence of adjacent teeth or implants due to unrestorable caries, residual roots, root fractures or orthodontic treatment
* Able (in the investigators opinion) and willing to comply with all study requirements
* Interested in tooth replacement with dental implants

Exclusion Criteria

* Endodontic periapical lesions with a diameter of more than 5 mm (radiographically determined)
* Sites with buccal and lingual bone plate loss more than 5 mm
* Frank purulence or acute abscess at the time of extraction
* Pregnancy or lactation
* Smokers or alcoholics
* Platelet dysfunction syndrome or thrombocytopenia
* Uncontrolled diabetes
* Medical contraindications to elective oral surgery procedures
Minimum Eligible Age

18 Years

Maximum Eligible Age

70 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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The University of Hong Kong

OTHER

Sponsor Role collaborator

The European Research Group on Periodontology (ERGOPerio)

NETWORK

Sponsor Role lead

Responsible Party

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Maurizio Tonetti

Executive Director, Clinical Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Maurizio Tonetti, DMD

Role: PRINCIPAL_INVESTIGATOR

The European Research Group on Periodontology (ERGOPerio)

Locations

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Faculty of Dentistry, The University of Hong Kong

Hong Kong, , Hong Kong

Site Status

Countries

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Hong Kong

References

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Reference Type DERIVED
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Other Identifiers

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HKUPhD20190528

Identifier Type: -

Identifier Source: org_study_id

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