Evaluation of Platelet Rich Fibrin on Reduction of Periodontal Problems After Surgical Removal of Mandibular Third Molar
This trial is active, not recruiting.
|Treatments||autologous platlet rich fibrin, one side in control group|
|Start date||December 2011|
|End date||April 2012|
|Trial size||30 participants|
|Trial identifier||NCT01583491, 900093|
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.
|Endpoint classification||efficacy study|
|Intervention model||parallel assignment|
|Masking||double blind (investigator, outcomes assessor)|
prf insert into surgical site immediate after surgery
Measurement of periodontal pocket depth at mid buccal, disto buccal and distolingual of mandibular second molar
time frame: 4 months
Male or female participants from 18 years up to 35 years old.
Inclusion Criteria: - have 2 impacted third molars Exclusion Criteria: - periodontal disease - history of periodontal surgery
|Official title||Evaluation of Platelet Rich Fibrin Efficacy on Reduction of Periodontal Problems|
|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.|
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