Bone Graft Particle Size on Bone Vitality and Volume
Primary Purpose
Bilateral Sinus Pneumatization, Posterior Maxillary Ridge Atrophy Due to Extraction
Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Puros allograft
Sponsored by
About this trial
This is an interventional treatment trial for Bilateral Sinus Pneumatization focused on measuring Sinus floor augmentation, Bone graft, Allograft, Dental implants, Maxillary sinus
Eligibility Criteria
Inclusion Criteria:
- Good physical health
- Capable of maintaining good oral hygiene
- Missing posterior maxillary teeth on both sides and less than 5 mm of residual jaw bone requiring maxillary sinus augmentation prior to dental implant placement
- Capable and willing to give informed consent
Exclusion Criteria:
- The presence of underlying medical conditions that may pose an undue risk for sinus surgery
- Patients with untreated oral infections
- Pregnant and lactating females
- Individuals who have the habit of smoking and/or tobacco chewing
- Patients not willing to participate in the study
Sites / Locations
- Department of Periodontology and Implant DentistryRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Bone Graft A
Bone Graft B
Arm Description
Bone Graft A: Mixture of 25% small-particle cortical, 25% large particle cortical, 25% small particle cancellous, 25% large particle cancellous allograft
Bone Graft B: 100% large particle cancellous allograft
Outcomes
Primary Outcome Measures
Quality of bone
Assessment of the quality of bone that is generated in the grafted sinuses by measuring the: percent vital bone formation, percent of inflammatory tissue if any
Quality of bone
Assessment of the quality of bone that is generated in the grafted sinuses by measuring the: percent of residual bone graft material
Quality of bone
Assessment of the quality of bone that is generated in the grafted sinuses by measuring the: percent of inflammatory tissue if any
Secondary Outcome Measures
Bone volume stability
Assessment of bone volume stability through CBCT analysis comparing it from the time of placement, 8 months post-grafting and 1 year post-implantation
Full Information
NCT ID
NCT04778709
First Posted
January 30, 2021
Last Updated
February 28, 2021
Sponsor
NYU College of Dentistry
1. Study Identification
Unique Protocol Identification Number
NCT04778709
Brief Title
Bone Graft Particle Size on Bone Vitality and Volume
Official Title
A Randomized, Split Mouth Study of the Effects of Bone Graft Particle Size on Bone Vitality and Bone Volume Outcomes in Subjects Undergoing Sinus Augmentation for the Placement of Dental Implants
Study Type
Interventional
2. Study Status
Record Verification Date
February 2021
Overall Recruitment Status
Recruiting
Study Start Date
November 13, 2020 (Actual)
Primary Completion Date
September 2021 (Anticipated)
Study Completion Date
September 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
NYU College of Dentistry
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Product Manufactured in and Exported from the U.S.
Yes
Data Monitoring Committee
No
5. Study Description
Brief Summary
To determine the effects of small and large bone graft particles vs large particles alone on percent vital bone, percent residual graft material, measured histologically from bone biopsies of the grafted site taken at the time of dental implant placement from subjects undergoing sinus augmentation for the placement of dental implants. Dental radiographs taken post operatively will be used to estimate bone graft volume differences between conditions.
Detailed Description
The proposed study is a Randomized, single-masked, split-mouth, single center study.
About 20 subjects will be screened in order to randomize 10 study subjects. 10 patients who needing bilateral sinus augmentation procedure using the lateral window technique will be randomized using computer generated randomized technique.
At the day of the surgical procedure each tooth sites will be randomized 1:1 into one of the following bone grafts to either the right or left side of the mouth.:
Bone graft A: A mixture of 25% small-particle cortical allograft, 25% large-particle cortical allograft, 25% small-particle cancellous allograft, and 25% large-particle cancellous allograft is used for one sinus (N=10)
Bone graft B: 100% large particle cancellous allograft for the contralateral sinus (N=10) Immediately after the sinus augmentation surgery a CBCT will be acquired and will be compared to a second CBCT prior to implant placement in order to compare the volumetric changes in the sinus.
At the visit of implant placement, a bone core will be collected from both sinuses for histomorphometric evaluation to evaluate the residual graft particles, the new vital bone formation and the amount of soft tissue components.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Bilateral Sinus Pneumatization, Posterior Maxillary Ridge Atrophy Due to Extraction
Keywords
Sinus floor augmentation, Bone graft, Allograft, Dental implants, Maxillary sinus
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Model Description
Each subject will receive bilateral sinus augmentation. Right and left sinuses will be randomly assigned to Bone Graft A and Bone Graft B.
Masking
ParticipantOutcomes Assessor
Masking Description
CBCT review, core biopsy evaluation and histomorphometry will be performed by a masked investigator.
Allocation
Randomized
Enrollment
10 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Bone Graft A
Arm Type
Experimental
Arm Description
Bone Graft A: Mixture of 25% small-particle cortical, 25% large particle cortical, 25% small particle cancellous, 25% large particle cancellous allograft
Arm Title
Bone Graft B
Arm Type
Active Comparator
Arm Description
Bone Graft B: 100% large particle cancellous allograft
Intervention Type
Device
Intervention Name(s)
Puros allograft
Intervention Description
Bilateral sinus augmentation procedure using the lateral window technique. Graft material combination A or B will be randomly assigned to right and left sinus.
Each subject will receive the following bone allograft material:
Four to six grams of commercially available human donor bone allograft (Puros Allograft Bone Particles, Zimmer Biomet, Palm Beach Gardens, FL USA) consisting of Graft A cortical and cancellous bone chips of both 250-1000 microns and 1000-2000 microns size, or Graft B for contralateral sinus: cancellous 1000-2000 microns size alone.
Primary Outcome Measure Information:
Title
Quality of bone
Description
Assessment of the quality of bone that is generated in the grafted sinuses by measuring the: percent vital bone formation, percent of inflammatory tissue if any
Time Frame
After surgery, 8 months, 1 year
Title
Quality of bone
Description
Assessment of the quality of bone that is generated in the grafted sinuses by measuring the: percent of residual bone graft material
Time Frame
After surgery, 8 months, 1 year
Title
Quality of bone
Description
Assessment of the quality of bone that is generated in the grafted sinuses by measuring the: percent of inflammatory tissue if any
Time Frame
After surgery, 8 months, 1 year
Secondary Outcome Measure Information:
Title
Bone volume stability
Description
Assessment of bone volume stability through CBCT analysis comparing it from the time of placement, 8 months post-grafting and 1 year post-implantation
Time Frame
After surgery, 8 months, 1 year
10. Eligibility
Sex
All
Minimum Age & Unit of Time
25 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Good physical health
Capable of maintaining good oral hygiene
Missing posterior maxillary teeth on both sides and less than 5 mm of residual jaw bone requiring maxillary sinus augmentation prior to dental implant placement
Capable and willing to give informed consent
Exclusion Criteria:
The presence of underlying medical conditions that may pose an undue risk for sinus surgery
Patients with untreated oral infections
Pregnant and lactating females
Individuals who have the habit of smoking and/or tobacco chewing
Patients not willing to participate in the study
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Edgard El Chaar, DDS, MS
Phone
212 998-9986
Email
ese1@nyu.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Aikaterini Georgantza, DDS
Phone
212-998-9730
Email
ag4222@nyu.edu
Facility Information:
Facility Name
Department of Periodontology and Implant Dentistry
City
New York
State/Province
New York
ZIP/Postal Code
10010
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Edgard El Chaar, DDS, MS
Phone
212-998-9986
Email
ese1@nyu.edu
First Name & Middle Initial & Last Name & Degree
Aikaterini Georgantza, DDS
Phone
212-998-9730
Email
ag4222@nyu.edu
First Name & Middle Initial & Last Name & Degree
Edgard El Chaar, DDS, Ms
12. IPD Sharing Statement
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Bone Graft Particle Size on Bone Vitality and Volume
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