NCT01212601
Completed
N/A
A Multicenter, Observational, Non-interventional Registry Designed to Collect Clinical Data in Chinese Patients Who Have Received CUBICIN® Treatment Under Condition of Actual Usage in Clinical Practice
ConditionsS. Aureus Bloodstream Infection
Overview
- Phase
- N/A
- Intervention
- Not specified
- Conditions
- S. Aureus Bloodstream Infection
- Sponsor
- AstraZeneca
- Enrollment
- 203
- Locations
- 1
- Primary Endpoint
- AEs of CUBICIN therapy
- Status
- Completed
- Last Updated
- 13 years ago
Overview
Brief Summary
This is a Multicenter, observational, non-interventional registry designed to collect clinical data in Chinese patients who have received CUBICIN treatment under condition of actual usage in clinical practice.
Detailed Description
MC MD
Investigators
Eligibility Criteria
Inclusion Criteria
- •Patient has received CUBICIN treatment, decided by treating physician
- •A patient who is considered as ethnic Chinese
- •Provision of subject informed consent
Exclusion Criteria
- •A patient record will not be eligible for the registry database if the patient received CUBICIN as part of a controlled clinical study for the current infection episode.
Outcomes
Primary Outcomes
AEs of CUBICIN therapy
Time Frame: 2 weeks
clinical response of CUBICIN therapy at each available time point
Time Frame: 2 weeks
Secondary Outcomes
- CPK level monitoring and results(2 weeks)
- treatment duration(2 weeks)
- Time to clinical response(2 weeks)
Study Sites (1)
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