GM-CSF to Decrease ICU Acquired Infections
NCT02361528
Infections, Inflammation
Amiens, France
View Trial DetailsNCT Number: NCT01523717
The purpose of this study is to investigate the relationship between a procalcitonin decrease over 72 hours and outcome in patients who have severe sepsis or septic shock.
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Notify Me18 year and older
All sexes
Observational
University of California Davis Health System, Sacramento, California, United States
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Time frame: within 28 day safter inlclusion
participants will be followed up for 28 days
Time frame: mortality during hospital stay
count all death through out stay in the hospital
Brahms AG
Industry
Procalcitonin Decrease Over 72 Hours and Outcome in Patients With Severe Sepsis or Septic Shock
Acronym: MOSES
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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