Maxillary Sinus Elevation With Bio-Oss or Straumann BoneCeramic

Status Completed

Clinical Trial Summary

The purpose of the study was to test a clinically relevant non-inferiority of Straumann BoneCeramic treatment compared to Bio-Oss treatment 180 to 240 days after sinus grafting procedure.

Clinical Trial Description

This is a prospective, controlled, randomised, multicenter study. The total study duration for each patient should be three years.

In total 13 visits per patient are scheduled in this study.

The study device Straumann Bone Ceramic is CE-marked.

Height centers in Italy will participate. ;

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT00901121
Study type	Interventional
Source	Institut Straumann AG
Contact
Status	Completed
Phase	N/A
Start date	July 2005
Completion date	March 2011

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