Extraction of Impacted 3rd Molars, Can Bone Support of the Second Molar be Promoted by a Bio-Oss Graft?
Primary Purpose
Impacted Third Molar Tooth
Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Geistlich Bio Oss
Sponsored by
About this trial
This is an interventional supportive care trial for Impacted Third Molar Tooth
Eligibility Criteria
Inclusion Criteria:
- Bilateral impacted 3rd molars.
- Healthy individuals
Exclusion Criteria:
- Smokers
- Alcohol abusers
- Pregnancy
Sites / Locations
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
3rd molar
Arm Description
Drug: Geistlich Bio Oss
Outcomes
Primary Outcome Measures
Mobility (Scale 0,1,2,3), change is being assessed.
Mobility will be assessed in the intervals mentioned above, and compared over time.
Pocket Depth (mm), change is being assessed.
Pocket depth will be assessed in the intervals mentioned above, and compared over time.
Secondary Outcome Measures
Full Information
NCT ID
NCT02753439
First Posted
March 20, 2016
Last Updated
April 25, 2016
Sponsor
The Baruch Padeh Medical Center, Poriya
Collaborators
Geistlich Pharma AG
1. Study Identification
Unique Protocol Identification Number
NCT02753439
Brief Title
Extraction of Impacted 3rd Molars, Can Bone Support of the Second Molar be Promoted by a Bio-Oss Graft?
Official Title
Extraction of Impacted 3rd Molars, Can Bone Support of the Second Molar be Promoted by a Bio-Oss Graft?
Study Type
Interventional
2. Study Status
Record Verification Date
March 2016
Overall Recruitment Status
Unknown status
Study Start Date
February 2017 (undefined)
Primary Completion Date
February 2018 (Anticipated)
Study Completion Date
February 2019 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
The Baruch Padeh Medical Center, Poriya
Collaborators
Geistlich Pharma AG
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
A prospective study examining bilateral 3rd molar extraction, by a split mouth protocol the investigators augment unilaterally and compare periodontal parameters in between.
Detailed Description
40 patients will undergo bilateral 3rd molar extractions, in each patient one side would be augmented by a "Bio-Oss" xenograft.
Post operative, periodontal parameters such as pocket depth and mobility will be evaluated and compared.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Impacted Third Molar Tooth
7. Study Design
Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
40 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
3rd molar
Arm Type
Experimental
Arm Description
Drug: Geistlich Bio Oss
Intervention Type
Drug
Intervention Name(s)
Geistlich Bio Oss
Other Intervention Name(s)
Bone Support
Intervention Description
Extraction of Impacted 3rd Molars,
Primary Outcome Measure Information:
Title
Mobility (Scale 0,1,2,3), change is being assessed.
Description
Mobility will be assessed in the intervals mentioned above, and compared over time.
Time Frame
Pre opp (base line), 1 month post opp, 3 months post opp, 6 months post opp
Title
Pocket Depth (mm), change is being assessed.
Description
Pocket depth will be assessed in the intervals mentioned above, and compared over time.
Time Frame
Pre opp (base line), 1 month post opp, 3 months post opp, 6 months post opp
10. Eligibility
Sex
All
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Bilateral impacted 3rd molars.
Healthy individuals
Exclusion Criteria:
Smokers
Alcohol abusers
Pregnancy
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Extraction of Impacted 3rd Molars, Can Bone Support of the Second Molar be Promoted by a Bio-Oss Graft?
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