NCT00901121

Maxillary Sinus Elevation With Bio-Oss or Straumann BoneCeramic

Maxillary Sinus Grafting With Bio-Oss or Straumann Bone Ceramic Followed by Delayed Placement of Straumann Dental Implants: A Comparative Histomorphometric and Clinical Study

• Status: Completed
• Phase: N/A
• Study type: Interventional
• Enrollment: 48 (actual)
• Sponsor: Institut Straumann AG · Industry
• Sex: All
• Age: 18 Years – 70 Years
• Healthy volunteers: Not accepted

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.

Detailed 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.

Conditions

• Teeth Loss
• Bone Loss

Interventions

Type	Name	Description
DEVICE	Straumann BoneCeramic	Straumann BoneCeramic (500-1000 microns, 0.5g)
DEVICE	Bio-Oss	Bio-Oss spongiosa granules, size of particle 0.25-1 mm

Timeline

• Start date: 2005-07-01
• Primary completion: 2007-04-01
• Completion: 2011-03-01
• First posted: 2009-05-13
• Last updated: 2016-03-03

Locations

8 sites across 1 country: Italy