Bone Graft Particle Size on Bone Vitality and Volume

Bilateral Sinus Pneumatization Clinical Trial

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

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT04778709
• Other study ID #: 19-00996
• Status: Terminated
• Phase: N/A
• Start date: November 13, 2020
• Est. completion date: February 1, 2022

Study information

• Verified date: November 2023
• Source: NYU College of Dentistry
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial 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.

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.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 4
• Est. completion date: February 1, 2022
• Est. primary completion date: February 1, 2022
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 25 Years to 65 Years

Eligibility

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

Related Conditions & MeSH terms

• Atrophy
• Bilateral Sinus Pneumatization
• Posterior Maxillary Ridge Atrophy Due to Extraction

Intervention

Device:
• Puros allograft
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.

Locations

Country	Name	City	State
United States	Department of Periodontology and Implant Dentistry	New York	New York

Sponsors (1)

Lead Sponsor	Collaborator
NYU College of Dentistry

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	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	After surgery, 8 months, 1 year
Primary	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	After surgery, 8 months, 1 year
Primary	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	After surgery, 8 months, 1 year
Secondary	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	After surgery, 8 months, 1 year