Clinical Trial Record

Return to Clinical Trials

Hot AXIOS System Japan Post Market Survey


2019-01-15


2020-10-30


2020-10-30


120

Study Overview

Hot AXIOS System Japan Post Market Survey

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

N/A

  • Pancreatic Pseudocyst Infection
  • Pancreatic Pseudocyst
  • Walled Off Necrosis Infection
  • Walled Off Necrosis
  • DEVICE: EUS-guided fistulization AXIOS
  • E7121

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates Results Reporting Dates Study Record Updates

2018-09-25  

N/A  

2022-03-17  

2019-01-08  

N/A  

2022-03-18  

2019-01-09  

N/A  

2022-03  

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

Design Details

Primary Purpose:
N/A


Allocation:
N/A


Interventional Model:
N/A


Masking:
N/A


Arms and Interventions

Participant Group/ArmIntervention/Treatment
: AXIOS Patient

DEVICE: EUS-guided fistulization AXIOS

  • By using a convex type ultrasonic endoscope to form a fistula by gastrointestinal puncture, to perform various drainage.
Primary Outcome MeasuresMeasure DescriptionTime Frame
Safety (Adverse Events and Device Malfunction)From implant procedure to 7 days after removal
Placement successAXIOS stent is placed in an appropriate position using the delivery system.During implant procedure
Stent retentionAXIOS stent stays at the position where it was implanted during the implant procedure.From implant procedure to removal (a maximum of 60 days)
Stent lumen patencyThe lumen of AXIOS stent is patent, and it can be used for drainage etc.From implant procedure to removal (a maximum of 60 days)
Decreased cyst sizeFrom implant procedure to final observation (a maximum of 60 days)
Removal successAXIOS stent can be removed using standard endoscopic snares or forceps.Removal procedure (a maximum of 60 days after implant procedure)
Secondary Outcome MeasuresMeasure DescriptionTime Frame

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person’s general health condition or prior treatments.

Ages Eligible for Study:
ALL

Sexes Eligible for Study:

Accepts Healthy Volunteers:

    Inclusion Criteria:

  • Patient who received implant procedure using study device at Japanese site.

  • Exclusion Criteria:

  • NA

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

No publications available