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Evaluation of MT-12 Implant Survival and Marginal Bone Loss — 213CEIH2016  

Jaw, Edentulous, Partially Clinical Trial

Official title:
Evaluation of MT-12 Implant Survival and Marginal Bone Loss

Clinical Trial Summary

The trial is designed as a consecutive enrollment prospective one-center study. A minimum of 30 patients will be included in the study. At implant installation, the patient will be randomized to receive one of the two types of implants (Control: internal hexagon connection implants (CON.INT); Test: Morse taper connection implants (MT-12)). Samples of peri-implant crevicular fluid (PICF) and intrasulcular plaque will be collected at -21 (second-stage surgery), -14 (impressions), 0 (Baseline: prosthesis delivery), 7 days and 1, 3, 6, 12 months. Prosthesis will be fabricated and delivered as usual, i.e., approximately two weeks after the impressions are taken.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02975674
Study type Interventional
Source Universidad de Granada
Contact
Status Completed
Phase N/A
Start date November 2016
Completion date February 2021
View Details
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