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The research of Interventional radiological for acute and subacute superior mensenteric vein-portal vein thrombosis: a multi-center clinical study

The research of Interventional radiological for acute and subacute superior mensenteric vein-portal vein thrombosis: a multi-center clinical study

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100049017
Enrollment
Unknown
Registered
2021-07-19
Start date
2022-01-01
Completion date
Unknown
Last updated
2022-03-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute and subacute superior mensenteric

Interventions

experimental group:Transcatheter arterial thrombolysis

Sponsors

The First Medical Center, Chinese PLA General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18 to 75 years; 2. The diagnosis of acute-subacute PV-SMV thrombus was confirmed by contrast-enhanced abdominal CT (acute phase [<=7 days], CT showed low density, and transition to subacute phase (7-14 days) showed high density); 3. Accompanied by abdominal pain, abdominal distension, nausea, anorexia, vomiting, fever and other symptoms, the course of the disease is within 14 days; 4. Abdominal symptoms (mainly abdominal pain) did not improve or worsened after 24 hours of intravenous anticoagulation therapy, extensive thrombosis and expected intestinal necrosis were more likely; 5. There are no other contraindications for angiography (such as iodine contrast agent allergy, uncontrolled infection, uncorrectable coagulation skills disorder, etc.); 6. The subjects voluntarily joined the study, signed the informed consent, and were able to cooperate with the follow-up and complete the research project.

Exclusion criteria

Exclusion criteria: 1. Chronic SMV-PV (the course of disease is more than 14 days, and CT scan shows abdominal wall thrombosis, collateral formation, etc.); 2. Intestinal necrosis, intestinal perforation, gastrointestinal bleeding; 3. Severe abnormal liver function (ALT/AST>=4ULN, DBIL>=3ULN) 4. Those with severe heart, lung, kidney, brain and other underlying diseases who cannot tolerate interventional therapy; 5. Combined with active bleeding of other organs; 6. Bilateral Allen test positive.

Design outcomes

Primary

MeasureTime frame
disease control rate;

Countries

China

Contacts

Public ContactWang Maoqiang

The First Medical Center, Chinese PLA General Hospital

wangmq@vip.sina.com+86 10 66937190

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026