Trials / Completed
CompletedNCT06856655
Achieving Portal Access With Scorpion Post-Approval Study 2
A Retrospective Data Collection Evaluating Portal Vein Access Sets For Transjugular Intrahepatic Portosystemic Shunt (TIPS) Procedures
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 82 (actual)
- Sponsor
- Argon Medical Devices · Industry
- Sex
- All
- Age
- —
- Healthy volunteers
- Not accepted
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
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Scorpion Portal Vein Access Kit | Procedure/Surgery: Transjugular Intrahepatic Portosystemic Shunt (TIPS) |
Timeline
- Start date
- 2022-02-01
- Primary completion
- 2024-03-28
- Completion
- 2024-03-28
- First posted
- 2025-03-04
- Last updated
- 2025-03-04
Locations
1 site across 1 country: United States
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT06856655. Inclusion in this directory is not an endorsement.