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Clinical Assessment of Dental Implant — H2015-1  

Tooth Loss Clinical Trial

Official title:
Clinical and Radiographic Assessment of V3 Implant: A Randomized Controlled Trial

Clinical Trial Summary

Primary Endpoints : The implant survival and success rate of V3 and C1 implants will be compared. Implant success rate will be evaluated by measuring the peri-implant bone remodeling from baseline to 1 year post insertion. The hypothesis is those implant survival rates of the test (V3) and control group (C1) are similar and that test V3 implant allows less peri-implant bone loss. Secondary Endpoints : The thickness of hard tissue in the buccal aspect of the V3 and C1 implants will be compared. The bone thickness will be measured in cone beam computerized tomography (CBCT) on the day of implantation, 4 and at one year after the final restoration. The hypothesis is that V3 implant allows thicker bone dimension in the cervical area.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02591706
Study type Interventional
Source University of Liege
Contact
Status Completed
Phase N/A
Start date February 2, 2015
Completion date June 2019
View Details
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