Tobramycin Exposure From Active Calcium Sulfate Bone Graft Substitute

NCT01938417 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 12

Last updated 2013-09-11

No results posted yet for this study

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

  • Orthopedic Operations

Interventions

DRUG

tobramycin

Sponsors & Collaborators

  • University of Lausanne Hospitals

    lead OTHER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2006-10-31
Primary Completion
2008-03-31

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01938417 on ClinicalTrials.gov