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Achieving Portal Access With Scorpion Post-Approval Study 2

NCT06856655 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 82

Last updated 2025-03-04

No results posted yet for this study

Summary

Creation of the parenchymal tract between the portal vein and the hepatic vein is the most difficult and time consuming step in a TIPS procedure. The purpose of this study is to evaluate portal vein access sets during the TIPS procedure.

Conditions

  • Portal Hypertension
  • Liver Diseases
  • Ascites Hepatic
  • Hydrothorax
  • Vascular Diseases

Interventions

DEVICE

Scorpion Portal Vein Access Kit

Procedure/Surgery: Transjugular Intrahepatic Portosystemic Shunt (TIPS)

Sponsors & Collaborators

  • Argon Medical Devices

    lead INDUSTRY

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-02-01
Primary Completion
2024-03-28
Completion
2024-03-28
FDA Device
Yes

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

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 NCT06856655 on ClinicalTrials.gov