Trials / Terminated
TerminatedNCT05765253
Achieving Portal Access With Scorpion Post-Approval Study (APASS)
A Prospective, Multicenter, Randomized Study Evaluating Portal Vein Access Sets During Transjugular Intrahepatic Portosystemic Shunt (TIPS) Procedures
- Status
- Terminated
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 3 (actual)
- Sponsor
- Argon Medical Devices · Industry
- Sex
- All
- Age
- 18 Years
- 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 | Portal Vein Access with Scorpion or Scorpion X set |
| DEVICE | Cook Transjugular Liver Access Set | Portal Vein Access with Ring or Rosch-Uchida set |
| PROCEDURE | Transjugular Intrahepatic Portosystemic Shunt (TIPS) | Transjugular Intrahepatic Portosystemic Shunt (TIPS) |
Timeline
- Start date
- 2023-07-13
- Primary completion
- 2023-10-16
- Completion
- 2023-11-19
- First posted
- 2023-03-13
- Last updated
- 2024-12-11
- Results posted
- 2024-12-11
Locations
3 sites across 1 country: United States
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT05765253. Inclusion in this directory is not an endorsement.