Clin2
NCT05146336Possibly a fitRecruiting

CytoSorb registry for critically ill patients needing blood treatment

Septic ShockAcute Respiratory Distress SyndromeTraumaRhabdomyolysisCardiogenic ShockPancreatitisAcute on Chronic Liver FailureAcute Liver Failure

Part of Blood & lymphatic, Bones, joints & muscles, Digestive system, Heart & circulation, Infections, Injuries & trauma, Lungs & breathing, Mental health clinical trials.

This registry collects information about critically ill patients who receive the CytoSorb 300 mL blood treatment. It may help doctors better understand when the treatment works best and when it should not be used.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
3,000 people
Ages
Any age
Study type
Observational

Who can take part

  • Your care team plans to use (or already used) the CytoSorb 300 mL device
  • You or your legal representative can give consent to join this registry
  • The CytoSorb use is not only to remove blood thinners (anti-clotting medicines)
  • It is not only for heart surgery use during cardiac surgery
  • If a serious medical issue happens after consent that makes CytoSorb unsafe or inappropriate, you may not be able to continue

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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