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Atural history of Peri-pancreatic cOLlEctiONs in acute pancreatitis based on assessment of content with CECT and MRI.

Completed
Conditions
pancreatitis
10015674
Registration Number
NL-OMON33664
Lead Sponsor
Sint Antonius Ziekenhuis
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
25
Inclusion Criteria

• Age 18 years or above
• Acute pancreatitis: upper abdominal pain and serum lipase and/ or amylase levels 3 times the upper level of normal
• Written informed consent
• Patients with peripancreatic fluid collections on CECT > 3 cm in short axis.

Exclusion Criteria

• History or imaging signs of chronic or *acute on chronic* pancreatitis
• AP due to malignancy
• Pregnancy
• Contraindication for MRI imaging (for example pacemaker)
• Incapacitated subjects

Study & Design

Study Type
Observational non invasive
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
<p>The primary endpoint is the amount of solid debris as seen on initial MRI in<br /><br>relationship to the absorption rate of these collections.</p><br>
Secondary Outcome Measures
NameTimeMethod
<p>• Infectious complications (bacteremia, pneumonia, infected necrosis).<br /><br>• Length of hospital stay<br /><br>• Need for ICU admission<br /><br>• New onset organ failure (onset, extent and duration, see definitions section)<br /><br>• Length of ICU stay<br /><br>• Need for percutaneous drainage<br /><br>• Need for surgical or endoscopical necrosectomy<br /><br>• Quality of Life.</p><br>
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