K85.80
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: • Acute pancreatitis according to the S3 Guideline Pancreatitis of the German Society for Gastroenterology, Digestive and Metabolic Diseases (DGVS) • Moderate or severe acute pancreatitis according to the Atlanta Classification of 2013 • CRP = 100 mg/l up to 24 hours after symptom onset or CRP = 150 mg/l if the onset of symptoms was more than 24 hours ago • Written informed consent
Exclusion criteria
Exclusion criteria: • Age < 18 or = 80 years • Positive harmless acute pancreatitis score (HAPS) • Therapy-refractory shock • Pregnancy or breastfeeding • Participation in other interventional trials
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Safety and tolerability of CRP-apheresis in acute pancreatitis (incidence of expected and unexpected adverse effects of CRP-apheresis) | — |
Secondary
| Measure | Time frame |
|---|---|
| Course of the disease (Determination of laboratory parameters/diagnostic biomarkers/scores: • ALT, AST, gamma-GT, alkaline phosphatase, bilirubin, pro-calcitonin, CRP, leukocytes, hematocrit, creatinine, serum urea, eGFR, urine excretion • Modified CT severity index (MCTSI) • SAPS (Simplified Acute Physiology Score) • TISS (Therapeutic Intervention Scoring System) • BISAP score • Hospitalization • Presence and infection rate of pancreatic necrosis) | — |
Countries
Germany
Contacts
DIAKO Krankenhaus, Medizinische Klinik – Innere Medizin