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Clinical Trial Summary

A prospective, multi-center, single-arm study for unresectable malignant gastric outlet obstruction with EUS-guided double-balloon-occluded gastrojejunostomy bypass (EPASS)


Clinical Trial Description

Primary objective is to investigate the safety and effectiveness of the AXIOS™ lumen-apposing Metal Stent used in the EUS-guided double-balloon-occluded gastrojejunostomy bypass (EPASS) for the management of symptoms associated with gastric outlet obstruction (GOO) secondary to malignant unresectable neoplasm. Primary Endpoint is GOOSS 3 rate without MAE at 30 days post procedure. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05644951
Study type Interventional
Source Boston Scientific Corporation
Contact Ryo Konishi
Phone +81368537500
Email JapanClinicalTrials@bsci.com
Status Recruiting
Phase N/A
Start date December 23, 2022
Completion date July 31, 2025

See also
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