Viewing Study NCT06620315



Ignite Creation Date: 2024-10-26 @ 3:41 PM
Last Modification Date: 2024-10-26 @ 3:41 PM
Study NCT ID: NCT06620315
Status: COMPLETED
Last Update Posted: None
First Post: 2024-08-15

Brief Title: Comparison Between Primary and Secondary Implant Stability of Hybrid Versus Resorbable Blast Media RBM Surfaces Using Resonance Frequency Analysis
Sponsor: None
Organization: None

Study Overview

Official Title: Comparison Between Primary and Secondary Implant Stability of Hybrid Versus Resorbable Blast Media RBM Surfaces Using Resonance Frequency Analysis
Status: COMPLETED
Status Verified Date: 2024-08
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: No
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: IMPLANTSTABIL
Brief Summary: To compare primary stability during initial loading of implant and secondary stability after 12 weeks of implant loading which are denoted as ISQ value of Hybrid DIO UFII versus Resorbable blast media RBM Osstem TSII implant surfaces
Detailed Description: An approval from the hospital ethical committee will be obtained for this study As a protocol all patients presenting to Institute of Dentistry CMH Lahore Medical College will be examined in general OPD and those patients who fulfill the inclusion and exclusion criteria will be referred to Prosthodontics department After history complete oral examination and informed consent Patients will be divided into two groups by lottery method In Group 1 Hybrid sand blasted acid etched implants will be place In Group 2 Resorbable Blast Media RBM implant surfaces will be placed On the basis of randomized study the patients will be selected for the study to measure implant primary stability with a resonance frequency analyzer at the time of initial loading of implant starting with an assessment immediately following implant placement with insertion torque of 30 Ncm and then secondary stability at 12 weeks post operatively by using Ostell Mentor This instrument on each implant by inserting a standardized abutment Smartpeg of fixed length into each implant The transducer probe Osstell mentor probe will be held so that the probe tip was aimed at the small magnet on top of the Smartpeg at a distance of 2-3 mm in both the buccal and lingual directions and the mean of these measurements will then be calculated The probe will be held still during the pulsing time until the instrument beeped and the displayed the ISQ value ISQ1 will be evaluated immediately during initial implant loading which will be primary stability and ISQ2 will be evaluated after 12 weeks of implant placement when implant is properly osseointegrated which will be secondary stability of an implant

The implant fixtures will be DIO UF II for the Hybrid implants and the Osstem TSII plus system for the RBM implants Data would be stratified for age gender and implant site to address the effect modifiers

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None