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ENROLLING BY INVITATION
NCT04814693
NA

Conventional Endoscopic Techniques Versus EndoRotor® System for Necrosectomy of Walled of Necrosis

Sponsor: Erasmus Medical Center

View on ClinicalTrials.gov

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

DEVICE

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.

PROCEDURE

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