Electromagnetic Positioning-Assisted Ultrasound Guidance in Transjugular Intrahepatic Portosystemic Shunt (TIPS)
1 other identifier
interventional
20
0 countries
N/A
Brief Summary
Transjugular intrahepatic portosystemic shunt (TIPS) is an important method for treating complications related to portal hypertension. The difficulty of its surgical procedures lies in portal vein puncture. Improper operation may lead to complications such as hepatic artery hemorrhage, hepatic capsular hemorrhage, and biliary tract hemorrhage. At present, the means of guiding portal vein puncture are limited. There is evidence supporting that ultrasound guidance can help reduce the number of punctures and lower the radiation dose, etc. However, ordinary ultrasound is limited by the influence of dimensions and can only guide punctures in the same plane, with limited guiding value. The use of the Imedis9000 magnetic navigation system can guide percutaneous vascular puncture in multiple dimensions, which can increase the success rate of puncture and shorten the operation time. This study conducted a prospective, single-arm study. The Imedis9000 magnetic navigation system was used for real-time positioning to guide precise TIPS stent implantation. The number of punctures, puncture success rate, stent implantation success rate, and the incidence of adverse events were evaluated to determine the application value of the Imedis9000 magnetic navigation system in TIPS procedure.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started May 2025
Shorter than P25 for not_applicable
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
May 13, 2025
CompletedFirst Posted
Study publicly available on registry
May 20, 2025
CompletedStudy Start
First participant enrolled
May 31, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 30, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
December 31, 2025
CompletedMay 20, 2025
May 1, 2025
4 months
May 13, 2025
May 13, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Success rate of portal vein puncture
Puncture success rate = Number of successful cases/total number of cases ×100%.
During TIPS procedure
Study Arms (1)
TIPS procedure under ultrasound combined with electromagnetic positioning guidance
EXPERIMENTALInterventions
TIPS procedure under ultrasound combined with electromagnetic positioning guidance
Eligibility Criteria
You may qualify if:
- Age≥18 years old;
- Including but not limited to patients requiring TIPS for: acute esophageal/gastric variceal bleeding, portal hypertensive gastropathy, cirrhotic ascites, cirrhotic hydrothorax, hepatorenal syndrome, Budd-Chiari syndrome, atypical portal hypertension, portal vein thrombosis, prevention of recurrent esophageal/gastric variceal bleeding, or prevention of recurrent ectopic variceal bleeding;
- Deemed by clinicians to require Transjugular Intrahepatic Portosystemic Shunt (TIPS)
- Voluntarily signed informed consent form
You may not qualify if:
- Severe right heart failure, congestive heart failure (ejection fraction \<40%), or severe valvular heart disease;
- Persistent severe pulmonary hypertension (mean pulmonary artery pressure \>45 mmHg) despite treatment;
- Uncontrolled systemic infection or inflammation;
- Hepatic encephalopathy stage III-IV;
- Presence of cardiac pacemaker, metallic implants, or other conditions susceptible to electromagnetic interference;
- Pregnancy or lactation;
- Poor visualization of the portal venous system on ultrasound;
- Investigator-determined unsuitability for study participation.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
May 13, 2025
First Posted
May 20, 2025
Study Start
May 31, 2025
Primary Completion
September 30, 2025
Study Completion
December 31, 2025
Last Updated
May 20, 2025
Record last verified: 2025-05