CompletedNot applicableNCT00559130
Efficacy Study of CytoSorb Hemoperfusion Device on IL-6 Removal in ARDS/ALI Patients With Sepsis
Studying Acute lung injury
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- MedaSorb Technologies, Inc
- Principal Investigator
- Martin K Kuhlmann, Prof. Dr.Vivantes Klinikum
- Intervention
- CytoSorb Hemoperfusion(device)
- Enrollment
- 100 enrolled
- Eligibility
- 18-80 years · All sexes
- Timeline
- 2007 – 2011
Study locations (6)
- Aachen, Germany
- Berlin, Germany
- Bonn, Germany
- Erfurt, Germany
- Göttingen, Germany
- Kiel, Germany
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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