NCT02288182View on ClinicalTrials.gov

Randomized, Controlled Study to Compare Straumann® VivOss™ to Geistlich Bio-Oss® in Sinus Floor Augmentation.

NACompletedINTERVENTIONAL
Enrollment

52

Participants

Timeline

Start Date

October 31, 2014

Primary Completion Date

October 31, 2017

Study Completion Date

February 28, 2018

Conditions
Healthy
Interventions
DEVICE

Straumann VivOss

Patients will receive Straumann VivOss for sinus augmentation.

DEVICE

Geistlich Bio-Oss

Patients will receive Geistlich Bio-Oss for sinus augmentation.

Trial Locations (2)

8032

University of Zürich, Zurich

78462

Zentrum für Implantologie, Parodontologie und 3D- Diagnostik, Konstanz

All Listed Sponsors
lead

Institut Straumann AG

INDUSTRY

NCT02288182 - Randomized, Controlled Study to Compare Straumann® VivOss™ to Geistlich Bio-Oss® in Sinus Floor Augmentation. | Biotech Hunter | Biotech Hunter