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Conventional Endoscopic Techniques Versus EndoRotor® System for Necrosectomy of Walled of Necrosis
Sponsor: Erasmus Medical Center
Summary
In acute pancreatitis, approximately 20% of the cases result in severe necrotizing pancreatitis which is associated with significant morbidity and mortality. Necrotizing pancreatitis is characterized by the development of an acute necrotic collection and as this collection persists beyond 4 weeks, walled off necrosis (WON) encapsulates the collection. To date, this is treated by the step-up approach, which contains percutaneous drainage and minimally invasive video assisted retroperitoneal debridement (VARD) or endoscopic ultrasound (EUS) guided drainage followed by direct endoscopic necrosectomy (DEN). Different DEN techniques are available for the treatment of WON, however, there is a lack of effective endoscopic instruments to perform DEN. Recently, the first dedicated alternative to conventional DEN has been cleared for use, namely the EndoRotor® Resection System. This device is a powered mechanical debridement device intended for use in endoscopic procedures to resect and remove necrotic debris during DEN for WON. Previous (pilot and feasibility) studies showed promising results in terms of the amount of procedures, adverse events and length of hospital stay. Therefore, aim of this study is to assess the performance of the EndoRotor, as compared to conventional endoscopic techniques, for direct endoscopic necrosectomy (DEN) of walled off necrosis (WON) in a randomized controlled trial.
Official title: A Prospective, Post-Market, Multicenter, Randomized Controlled Trial to Compare the Performance of the EndoRotor® System Versus Conventional Endoscopic Techniques for Direct Endoscopic Necrosectomy of Walled Off Necrosis - The RESOlVE Trial
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
INTERVENTIONAL
Enrollment
60
Start Date
2022-09-02
Completion Date
2027-02-01
Last Updated
2025-08-08
Healthy Volunteers
No
Interventions
EndoRotor® System (Interscope, Inc., Northbridge, MA USA),
The EndoRotor System is intended for use in endoscopic procedures to resect and remove necrotic debris during DEN for WON. DEN with the EndoRotor System (study device) is considered to be standard of care therapy for patients with WON and not investigational.
Conventional endoscopic devices (according to standards of care)
Endoscopic devices used to perform conventional DEN will be chosen according to standard of care and Investigator preference.
Locations (12)
University of Alabama Medical Center
Birmingham, Alabama, United States
California Pacific Medical Center
San Francisco, California, United States
Thomas Jefferson University Hospital
Philadelphia, Pennsylvania, United States
Copenhagen University Hospital
Hvidovre, Denmark
Evangelical Hospital
Düsseldorf, Germany
University of Frankfurt
Frankfurt, Germany
Humanitas Reserach Hospital & Humanitas University
Milan, Italy
Fondazione Policlinico Universitario Agostino Gemelli IRCCS
Roma, Italy
Charlotte van Veldhuisen
Amsterdam, Netherlands
Amsterdam University Medical Center
Amsterdam, Netherlands
St. Antonius Hospital
Nieuwegein, Netherlands
Central Manchester University Hospital
Manchester, United Kingdom