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Pancreatic Pseudocyst clinical trials

View clinical trials related to Pancreatic Pseudocyst.

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NCT ID: NCT04494282 Completed - Clinical trials for Pancreatic Duct Disorder

The Economic Impact of the Pancreatography in the Endoscopic Treatment of Pancreatic Pseudocysts

Start date: August 2015
Phase: N/A
Study type: Interventional

Pancreatic pseudocysts (PP) present as a complication that occurs in 5-15% of acute pancreatitis and 26-40% of chronic pancreatitis (1-3). To date the endoscopic drainage with endoscopic ultrasound (EUS) has replace the surgical treatment due to the similar success and complication rate but with a lower cost and short hospital stay (4-6). Regarding recurrence, it is important to know the anatomy of the main pancreatic duct (MPD). For this purpose, the endoscopic retrograde pancreatography (ERP) has been describe as a useful tool. In fact, many authors perform it before the endoscopic drainage while others wait several weeks after the drainage (7-9) with similar technical success (5,8). However, there are no studies that compare the technical difficulty and the total cost between these two approaches.

NCT ID: NCT03808272 Completed - Clinical trials for Pancreatic Pseudocyst and Walled-off Necrosis

AXIOS CHINA (E7148)

Start date: April 17, 2019
Phase: N/A
Study type: Interventional

To study the safety and effectiveness of the AXIOS Stent with Electrocautery Enhanced Delivery System for endoscopic trans enteric drainage of pancreatic pseudocyst and walled-off necrosis in Chinese population, to support the regulatory approval by CFDA

NCT ID: NCT03797209 Completed - Clinical trials for Pancreatic Pseudocyst

Hot AXIOS System Japan Post Market Survey

Start date: January 15, 2019
Phase:
Study type: Observational

To detect information of Adverse Events and Device Malfunctions under real world medical condition in Japan.

NCT ID: NCT03147768 Completed - Clinical trials for Pancreatic Neoplasms

Laser Tissue Welding - Distal Pancreatectomy Sealing Study

LTW
Start date: January 1, 2018
Phase: Phase 1
Study type: Interventional

The laser tissue welding device is intended for use in patients requiring sealing of the pancreas after partial pancreatectomy, and including those patients who are fully heparinized or have hemodilutional coagulation failure. The hypothesis is that the laser tissue welding device is safe and effective in sealing the pancreas, thereby decreasing the blood loss (operative and post-operative), and pancreatic juice leakage for patients when the Laser Tissue Welding device is used after pancreatic resection.

NCT ID: NCT03002051 Completed - Acute Cholecystitis Clinical Trials

EUS-guided Transenteric Drainage With a Novel Lumen-apposing Metal Stent

Start date: October 2016
Phase: N/A
Study type: Interventional

To evaluate clinical efficacy and safety of a novel lumen-apposing FCSEMS for EUS-guided transenteric drainage of PFC or of biliary tree including GB

NCT ID: NCT02730663 Completed - Clinical trials for Pancreatic Pseudocyst

A Study to Evaluate the Effectiveness and Safety of EUS-guided Transluminal Drainage With 'Niti-S SPAXUS Stent'

Start date: March 21, 2016
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the safety and effectiveness of endoscopic ultrasound (EUS)-guided transluminal drainage with 'Niti-S SPAXUS Stent' for the treatment of pancreatic pseudocyst.

NCT ID: NCT02146352 Completed - Clinical trials for Pancreatic Pseudocyst(s)

AXIOS Stent With Electrocautery Enhanced Delivery System

Start date: June 2014
Phase: N/A
Study type: Interventional

The purpose of this study is to demonstrate the safety and effectiveness of the AXIOS Stent with Electrocautery Enhanced Delivery System for endoscopic transenteric drainage of pancreatic pseudocysts.

NCT ID: NCT02041793 Completed - Clinical trials for Pancreatic Pseudocyst

Laparoscopic Cystogastrostomy Versus Endoscopic Cystogastrostomy

Start date: May 2010
Phase: N/A
Study type: Interventional

This study is a randomized controlled trial comparing Laparoscopic and endoscopic drainage for pseudocyst of the pancreas secondary to acute pancreatitis. The primary outcome measure will be resolution of the pseudocyst by the intended treatment within 4 weeks. The secondary outcomes will be complications, recurrence and cost analysis between the two methods.

NCT ID: NCT01419769 Completed - Clinical trials for Pancreatic Pseudocyst(s)

AXIOS Stent & Delivery System Study

Start date: August 2011
Phase: N/A
Study type: Interventional

The Xlumena AXIOS Stent and Delivery System is an investigational device in the USA, and this study is being conducted under an Investigational Device Exemption (IDE) granted by the US Food and Drug Administration (FDA). The study design is prospective, multi-center, non-blinded, single-arm (nonrandomized) study. Up to 10 sites in the United States, European Community and/or Japan will enroll a total of 24 patients. A majority of the patients will be enrolled in the United States. Patients will be followed at (approximately) 30 days and/or 60 days depending upon pseudocyst resolution confirmation, at 1-week post-stent removal,and possibly at 3 and 6 month post-stent removal.

NCT ID: NCT01384617 Completed - Pancreatic Cancer Clinical Trials

Trial Assessing Roux-en-Y Anastomosis of the Pancreatic Stump to Prevent Pancreatic Fistula Following Distal Pancreatectomy

Start date: June 2011
Phase: N/A
Study type: Interventional

The objective is to clarify Roux-en-Y anastomosis of the pancreatic stump decreases pancreatic fistula following distal pancreatectomy, compared with stapling closure of the pancreatic stump.