Status
Conditions
Treatments
About
The purpose of this study is to examine how Osseodensification, a well-defined bone preparation procedure utilizing special densifying burs (a tool to prepare bone) compares to the standard drilling procedure utilizing regular bone drills, to possibly enhance dental implant healing.
Full description
Our postulated null hypotheses is that implants placed with osseodensification surgical drilling compared to those placed with subtractive conventional drilling technique in a split-mouth design will result: 1) in the same insertion torque values and; 2) in the same implant stability quotient values when measured immediately after implant placement and after 1, 2, 3, 4, 5, 6, 7, 8, and 12 weeks.
Study Objectives:
A.Perform a prospective clinical study to investigate implant primary stability through measuring insertion torque values (IT) and Implant stability quotient (ISQ) when implants are placed using a standard drilling protocol (subtractive surgical drilling, as recommended by implant manufacturers) compared to osseodensification drilling protocol in a split-mouth design.
B.Implant stability quotient will be measured once the implant is placed (immediate), and at 1, 2, 3, 4, 5, 6, 7, 8, and 12 weeks.
C.To investigate, and analyze these two surgical drilling protocols as function of different implant manufacturers with variations in diameter and length.
D.To further track trends in the use of osseodensification surgical drilling once the patient receives the prosthodontic reconstruction.
E.To share the knowledge generated from this prospective analysis through scientific publications.
Patient selection will focus on the need of implant placement on the right and left equivalent sides of the maxilla/mandible where one side/site will receive implant(s) placed post osseodensification surgical drilling recommended by Densifying reference guide of the Densah Burs manufacturer, and the other side/site will receive implant(s) placed by the control technique, which is subtractive conventional drilling recommended by the specific implant manufacturer.
Written consent will be provided, explained and signed by participating patients.
After Dental Implant procedure, participating patients will be asked to participate in 6-12 weekly follow visits.
Subjects Selection and Study Procedures:
Study will include 23 patients. Patients should not be in another research study or have not been in any other research study in the last 90 days. They cannot be in this study if they are abusing any drugs.
Patient selection will focus on the need of implant placement on the right and left equivalent sides of the maxilla/ mandible where one side/site will receive implant(s) placed by osseodensification surgical drilling, and the other side/site will receive implant(s) placed by the control surgical technique, which is subtractive conventional drilling recommended by the implant manufacturer.
Written consent will be provided, explained and signed by participating patients.
After Dental Implant procedure, participating patients will be asked to participate in 6-12 weekly follow-up visits.
Subjects Selection and Study Procedures:
Study will include 23 patients. Patients should not be in another research study or have not been in any other research study in the last 90 days. They cannot be in this study if they are abusing any drugs.
Patient selection will focus on the need of implant placement on the right and left equivalent sides of the maxilla/mandible where one side/site will receive implant(s) placed by osseodensification surgical drilling according to the manufacturer Densifying Reference Guide, and the other side/site will receive implant(s) placed by the control surgical technique, which is subtractive conventional drilling recommended by the implant manufacturer.
Written consent will be provided, explained and signed by participating patients.
After Dental Implant procedure, participating patients will be asked to participate in 6-12 weekly follow visits.
Study Procedures:
Enrollment
Sex
Ages
Volunteers
Inclusion criteria
Exclusion criteria
23 participants in 2 patient groups
Loading...
Data sourced from clinicaltrials.gov
Clinical trials
Research sites
Resources
Legal