Clinical Trial of EPASS With Hot AXIOS System

NCT05644951 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 51

Last updated 2025-12-03

No results posted yet for this study

Summary

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

Conditions

  • Gastric Outlet Obstruction

Interventions

DEVICE

Hot AXIOS system used for EPASS

EUS-guided double-balloon-occluded gastrojejunostomy bypass with Hot AXIOS system

Sponsors & Collaborators

  • Boston Scientific Corporation

    lead INDUSTRY

Principal Investigators

  • Takao Itoi, MD · Tokyo Medical University Hospital

Study Design

Allocation
NA
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-12-23
Primary Completion
2024-12-05
Completion
2025-08-29

Countries

  • Japan

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05644951 on ClinicalTrials.gov