Evaluation of Platelet Rich Fibrin on Reduction of Periodontal Problems After Surgical Removal of Mandibular Third Molar

NCT ID: NCT01583491

Last Updated: 2012-04-25

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

UNKNOWN

Clinical Phase

PHASE4

Total Enrollment

30 participants

Study Classification

INTERVENTIONAL

Study Start Date

2011-12-31

Study Completion Date

2012-05-31

Brief Summary

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The purpose of this study is to determine the influence of platelet rich fibrin to reduction of periodontal problems after surgical removal of third molar.

Detailed Description

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After extraction or surgical removal of third molar, a deep bony pocket created behind the second molar specially in the mandible. For reduction of this problem, investigators, needed to acceleration tissue healing. For this purpose, investigators used platelet rich fibrin (autologous) and followed patient for 3 months.

Conditions

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Mastication Disorder

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

PREVENTION

Blinding Strategy

DOUBLE

Investigators Outcome Assessors

Study Groups

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prf group.peridontal problem

prf insert into surgical site immediate after surgery

Group Type ACTIVE_COMPARATOR

autologous platlet rich fibrin

Intervention Type PROCEDURE

one dose immediate after surgery

control group

Group Type PLACEBO_COMPARATOR

one side in control group

Intervention Type PROCEDURE

control group insert any things after surgery

Interventions

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autologous platlet rich fibrin

one dose immediate after surgery

Intervention Type PROCEDURE

one side in control group

control group insert any things after surgery

Intervention Type PROCEDURE

Other Intervention Names

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prf

Eligibility Criteria

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Inclusion Criteria

* have 2 impacted third molars

Exclusion Criteria

* periodontal disease
* history of periodontal surgery
Minimum Eligible Age

18 Years

Maximum Eligible Age

35 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Majid Eshghpour

OTHER

Sponsor Role lead

Responsible Party

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Majid Eshghpour

assistant professor

Responsibility Role SPONSOR_INVESTIGATOR

Other Identifiers

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900093

Identifier Type: -

Identifier Source: org_study_id

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