Clinical Trials Directory

Trials / Completed

CompletedNCT01938417

Tobramycin Exposure From Active Calcium Sulfate Bone Graft Substitute

Status
Completed
Phase
Study type
Observational
Enrollment
12 (actual)
Sponsor
University of Lausanne Hospitals · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This study aimed to assess the systemic absorption and disposition of tobramycin in patients treated with a tobramycin-laden bone graft substitute (Osteoset® T).

Conditions

Interventions

TypeNameDescription
DRUGtobramycin

Timeline

Start date
2006-10-01
Primary completion
2008-03-01
First posted
2013-09-10
Last updated
2013-09-11

Source: ClinicalTrials.gov record NCT01938417. Inclusion in this directory is not an endorsement.

Tobramycin Exposure From Active Calcium Sulfate Bone Graft Substitute (NCT01938417) · Clinical Trials Directory