Pancreatitis Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- You are either already using, or your doctors are planning for you to use, a specific medical device called CytoSorb® 300 mL (a blood-filtering device).
- You are willing and able to give your written agreement (consent) to take part in this registry study.
Who may not be able to join:
- The CytoSorb® 300 mL device is being used only to remove blood-thinning medications from your body (rather than for other treatment purposes).
- The CytoSorb® 300 mL device is being used only during heart surgery in the operating room, and not for any other purpose.
- After you have already given your consent to join, a complication or medical situation arises that means the CytoSorb® 300 mL device is no longer safe or suitable for you to use (confirm with trial site).
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Ricard Ferrer Roca, MD, Hospital Vall d'Hebron
Phone: +49 30 654 99 145
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
ICU mortality; In-hospital mortality
Can't join this trial?
Data last synced from ClinicalTrials.gov: 26 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.