Clinical Trials Directory

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UnknownNCT02504034

Interventional Radiology for the Treatment of Symptomatic Portal Hypertension in Patients With Cavernous Transformation of Portal Vein

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
150 (estimated)
Sponsor
Sun Yat-sen University · Academic / Other
Sex
All
Age
1 Year – 80 Years
Healthy volunteers
Not accepted

Summary

To evaluate the values of portosystemic shunt and other interventional radiology approaches for treatment of symptomatic portal hypertension in patients with cavernous transformation of portal vein.

Conditions

Interventions

TypeNameDescription
PROCEDURETranshepatic portosystemic shuntPortal vein (PV) was punctured with a 22-gauge chiba needle. A 0.018-inch guidewire was advanced through the needle into PV lumen. The needle was exchanged and a 6-French sheath inserted over the wire. Then middle hepatic vein (MHV) was punctured with a 20-gauge reformed needle through the transhepatic sheath. Another 0.018-inch guidewire was advanced through the needle into right internal jugular vein and then snared out of body. A 0.035-inch, 260-cm-long stiff shaft wire was introduced through the transjugular sheath and manipulated into main portal vein (MPV) and then into SMV. The parenchymal tract was dilated with balloon catheter, then one or more bare metal stents and one or more covered stents were inserted to line the parenchymal tract.
DEVICE6-French sheath
DEVICE22-gauge chiba needle
DEVICE260-cm-long stiff shaft wire
DEVICEBalloon catheter
DEVICEBare metal stent
DEVICECovered stent

Timeline

Start date
2010-10-01
Primary completion
2020-12-01
First posted
2015-07-21
Last updated
2015-07-21

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT02504034. Inclusion in this directory is not an endorsement.