Bone Level Tapered Multi-Center Study

Status Active, not recruiting

Clinical Trial Summary

The aim of this randomized, controlled, multi-center study is to assess the clinical and radiographic outcomes of using a Straumann® Bone Level Tapered implant for immediate implantation following extraction of a tooth in the pre-molar and anterior region of the maxilla and mandible (test) compared to the outcomes of placing this implant in healed sites (control).

Clinical Trial Description

The primary objective is to demonstrate that the change in mean peri-implant marginal bone level changes (mesial and distal) from loading to 12 months post-loading of the test treatment will not be worse than the control treatments. The secondary objectives of the study are to assess differences in clinical and radiographic outcomes between the test and control treatments at 12 months post-loading by looking at implant success and survival, buccal bone dimensional changes, implant stability, soft tissue changes, subject satisfaction, and adverse events. An additional objective is to assess long-term differences in clinical and radiographic outcomes, as measured in the primary and secondary objectives, over the span of two, three, four, and five years. ;

Study Design

Related Conditions & MeSH terms

Tooth Loss

Clinical Trial Details

NCT number	NCT02569671
Study type	Interventional
Source	Institut Straumann AG
Contact
Status	Active, not recruiting
Phase	N/A
Start date	March 2016
Completion date	March 2024

View Details

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