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Application of angiography parametric imaging (API) in evaluating hemodynamic changes in interventional diagnosis and treatment of portal hypertension

Application of angiography parametric imaging (API) in evaluating hemodynamic changes in interventional diagnosis and treatment of portal hypertension

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000035738
Enrollment
Unknown
Registered
2020-08-16
Start date
2020-10-01
Completion date
Unknown
Last updated
2020-08-17

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

Conditions

Portal Hypertension

Interventions

Sponsors

Zhongshan Hospital of Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. The gender of the patient is not limited, aged 18 to 75 years old; 2. Clinically or pathologically diagnosed liver cirrhosis; 3. A history of rupture of esophageal and gastric varices confirmed by endoscopy, and bleeding again after receiving standard treatment; 4. Child A or B grade of liver function; 5. Platelet count >=50x10^9/L; 6. Prothrombin time (PT) does not exceed the upper limit of the normal control for 3 seconds; 7. Serum creatinine concentration <=115umol/L; 8. The patient and family members agree to join the clinical trial and sign an informed consent form.

Exclusion criteria

Exclusion criteria: 1. Imaging confirmed extensive thrombosis in the portal system; 2. Those who have previously received portal hypertension surgery related treatments (including: splenectomy, surgical devascularization or shunt, etc.); 3. Those with any malignant tumor; 4. Pulmonary artery pressure>40mmHg, left ventricular ejection fraction =100, total bilirubin> 51umol/L that fails to improve after symptomatic treatment; combined with active infection, especially inflammation of the biliary system; female patients are pregnant Or breastfeeding; severe contrast agent allergy.

Design outcomes

Primary

MeasureTime frame
Time-to-peak;Peak Height;AUC;

Countries

China

Contacts

Public ContactJingqin Ma

Zhongshan Hospital of Fudan University

13818527709@163.com+86 13818527709

Outcome results

None listed

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