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NCT01583491 Clinical Trial

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

Mastication Disorder Clinical Trial

Official title:
Evaluation of Platelet Rich Fibrin Efficacy on Reduction of Periodontal Problems

Clinical Trial Details — Status: Active, not recruiting

Administrative data
NCT number NCT01583491
Other study ID # 900093
Secondary ID
Status Active, not recruiting
Phase Phase 4
First received December 7, 2011
Last updated April 24, 2012
Start date December 2011
Est. completion date May 2012

Study information
Verified date April 2012
Source Mashhad University of Medical Sciences
Contact n/a
Is FDA regulated No
Health authority Iran: Ethics Committee
Study type Interventional

Clinical Trial Summary

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.

Description:

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.

Recruitment information / eligibility
Status Active, not recruiting
Enrollment 30
Est. completion date May 2012
Est. primary completion date April 2012
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 35 Years
Eligibility Inclusion Criteria:

- have 2 impacted third molars

Exclusion Criteria:

- periodontal disease

- history of periodontal surgery

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Investigator, Outcomes Assessor), Primary Purpose: Prevention

Related Conditions & MeSH terms

Intervention

Procedure:
• autologous platlet rich fibrin
one dose immediate after surgery
• one side in control group
control group insert any things after surgery

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
Majid Eshghpour

Outcome
Type Measure Description Time frame Safety issue
Primary Measurement of periodontal pocket depth at mid buccal, disto buccal and distolingual of mandibular second molar 4 months Yes
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