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Evaluation of Integration Success and Crestal Bone Preservation Biomet 3i's T3 Implant System — OAK  

Partial Edentulism Clinical Trial

Official title:
A Prospective, Randomized-controlled Evaluation of Biomet 3i's T3 Implant System for Integration Success and the Preservation of Crestal Bone

Clinical Trial Summary

This study evaluates the T3 implant system for the preservation of alveolar crestal bone and the establishment of initial integration. The new surface-treated features of the implant may contribute to improved soft and hard tissue healing. The success rate of the T3 implant will be no different than that of the control implant, which possess similar geometry but different surface treatments.

Clinical Trial Description

This prospective, randomized-controlled study will enroll qualified patients with partial edentulism who will be treated with at least two dental implants. Implant sites will be randomly assigned to receive either a test (T3 implant) or control (Nanotite Certain Tapered implant) with an 80:20 (test:control) randomization ratio. All implants will be allowed to integrate without occlusal forces and final restorations will be cemented thereafter. Cumulative success rate and crestal bone regression of both treatment groups will be the primary and secondary study endpoints, respectively. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02161874
Study type Interventional
Source ZimVie
Contact
Status Completed
Phase N/A
Start date April 2013
Completion date July 2020
View Details
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