Clinical trial involving patients with indication of endoscopic drainage of Pancreatic Collections with the aim to compare rates of displacement of two type of prothesis: with and without anti-migration systems

Not Applicable

Recruiting

• Conditions: Pancreatic pseudocyst; acute necrotizing pancreatitis; organized pancreatic necrosis The study will be conducted in human volunteers of the intervention (endoscopic drainage with self-expandable metallic stent). Such pathologies must be due to a documented episode of acute pancreatitis causing compressive symptoms or clinical or laboratory or radiological signs of infection. However, it is mandatory that patients have clinical stability, without requiring cardiac inotropic support and/or vasopressors; K86.3; C23.550.717; C06.689.750.650; C04.182.640.692

• Registration Number: RBR-4mdb59
• Lead Sponsor: Hospital das clínicas da Universidade de Sao Paulo

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2019-10-09
• Last Update Posted: 29 May 2023

Recruitment & Eligibility

• Status: Recruiting
• Sex: Not specified
• Target Recruitment: Not specified

Inclusion Criteria

Patients of any age; any gender; with the diagnosis of fluid pancreatic collection with definite ethiology of acute pancreatitis identified by abdominal radiological study after 4 weeks of onset of acute event; with symptoms such as pain or compression of the intra-abdominal organs by the collection or infected collections or causing sepsis

Exclusion Criteria

Patient who refuses to sign the informed consent;pancreatic fluid collection with less than 4 weeks after acute pancreatis;Cystic Formation less than 6 centimeters and without symptoms;
food residues in the stomach during endoscopic exam;collection distant from the pancreas that prohibit endoscopic drainage because because it has no contact with the stomach or duodenum; evidence of bleeding inside of the collection; septic shock defined as an abdominal sepsis that does not respond to intravenous fluid and requires cardiac inotropic support or vasopressors

Study & Design

• Study Type: Intervention
• Study Design: Not specified