A Study of Auxora in Patients With Acute Pancreatitis and Accompanying SIRS
NCT04681066
Acute Pancreatitis, Digestive System Diseases
Long Beach, California, United States
View Trial DetailsNCT Number: NCT03028181
The study aims to assess and analyze some selected antioxidants and laboratory parameters during hospitalization of the patients with acute pancreatitis. It will allow to better understanding of the mechanisms of disease and the development of better diagnostic, treatment and monitoring.
It is an observational diagnostic study and does not involve any additional administration of medicinal substances, modification of treatment or dropping the use of routine methods of treatment of a disease. The study procedure includes detailed personal medical history as separate document like as a routine medical interview, and three times taking a small amount of venous blood (together about 15 ml), in the first, third, and seventh day of hospitalization (in the case of longer hospital treatment).
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Observational
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: 3 weeks
Time frame: 2 weeks
Time frame: 12 months
Time frame: 3 months
Time frame: 2 months
Time frame: 1 months
Time frame: 3 months
Time frame: 3 weeks
Time frame: 3 weeks
Time frame: 3 months
Time frame: 3 weeks
Time frame: 2 months
Time frame: 1 month
Time frame: 1 month
Time frame: 1 month
Time frame: 2 weeks
Time frame: 3 months
Looking for future studies?
Notify MeWroclaw Medical University
Other
The Evaluation of Pro/Antioxidative Profile and Diagnostic Parameters in the Patients With Acute Pancreatitis
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