Evaluation of Platelet Rich Fibrin on Reduction of Periodontal Problems After Surgical Removal of Mandibular Third Molar
This study is ongoing, but not recruiting participants.
Sponsor:
Majid Eshghpour
Information provided by (Responsible Party):
Majid Eshghpour, Mashhad University of Medical Sciences
ClinicalTrials.gov Identifier:
NCT01583491
First received: December 7, 2011
Last updated: April 24, 2012
Last verified: April 2012
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Purpose
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.
| Condition | Intervention | Phase |
|---|---|---|
|
Mastication Disorder |
Procedure: autologous platlet rich fibrin Procedure: one side in control group |
Phase 4 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Efficacy Study Intervention Model: Parallel Assignment Masking: Double Blind (Investigator, Outcomes Assessor) Primary Purpose: Prevention |
| Official Title: | Evaluation of Platelet Rich Fibrin Efficacy on Reduction of Periodontal Problems |
Further study details as provided by Mashhad University of Medical Sciences:
Primary Outcome Measures:
- Measurement of periodontal pocket depth at mid buccal, disto buccal and distolingual of mandibular second molar [ Time Frame: 4 months ] [ Designated as safety issue: Yes ]
| Enrollment: | 30 |
| Study Start Date: | December 2011 |
| Estimated Study Completion Date: | May 2012 |
| Estimated Primary Completion Date: | April 2012 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Active Comparator: prf group.peridontal problem
prf insert into surgical site immediate after surgery
|
Procedure: autologous platlet rich fibrin
one dose immediate after surgery
Other Name: prf
|
| Placebo Comparator: control group |
Procedure: one side in control group
control group insert any things after surgery
|
Detailed 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.
Eligibility| Ages Eligible for Study: | 18 Years to 35 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | Yes |
Criteria
Inclusion Criteria:
- have 2 impacted third molars
Exclusion Criteria:
- periodontal disease
- history of periodontal surgery
Contacts and Locations
No Contacts or Locations Provided
More Information
No publications provided
| Responsible Party: | Majid Eshghpour, assistant professor, Mashhad University of Medical Sciences |
| ClinicalTrials.gov Identifier: | NCT01583491 History of Changes |
| Other Study ID Numbers: | 900093 |
| Study First Received: | December 7, 2011 |
| Last Updated: | April 24, 2012 |
| Health Authority: | Iran: Ethics Committee |
Keywords provided by Mashhad University of Medical Sciences:
|
platelet rich fibrin mandibular third molar periodontal problem |
ClinicalTrials.gov processed this record on May 23, 2013