CompletedNCT00811629
Influence of Acute Respiratory Distress Syndrome (ARDS) and Severe Sepsis on sRAGE Levels in ICU Patients
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
- University Hospital, Clermont-Ferrand
- Principal Investigator
- Matthieu JABAUDON, MDUniversity Hospital, Clermont-Ferrand
- Intervention
- sRAGE(other)
- Enrollment
- 60 enrolled
- Eligibility
- 18-95 years · All sexes
- Timeline
- 2009 – 2009
Study locations (1)
- CHU Clermont-Ferrand, Clermont-Ferrand, France
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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