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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05596253
Other study ID # HF-TIPS
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date October 11, 2022
Est. completion date July 2025

Study information

Verified date April 2024
Source West China Hospital
Contact Xuefeng Luo
Phone +86 18980606826
Email luo_xuefeng@yeah.net
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of this study is to conduct a prospective trial to investigate the incidence of heart failure in cirrhosis patients undergoing transjugular intrahepatic portosystemic shunt ,and to analyze the the predictors and modififications of cardiac function.


Description:

Hyperdynamic circulation is a common Phenomenon in cirrhosis due to systemic and splanchnic vasodilatation, which may result cardic dysfunction and abnormal structure ,called cirrhotic cardiomyopathy(CCM). Transjugular intrahepatic portosystemic shunt (TIPS), as a effective technique to alleviates portal hypertension in cirrhotic patients, often be used to treat with refractory ascites and variceal bleeding which endoscopy and drug therapy are ineffective. However, owing to the increased shunting of blood from the splanchnic vascular bed into the central vascular bed, TIPS further exacerbates the hyperdynamic circulatory state, which may lead to heart failure.yet there are no convincing research to study the incidence of heart failure in cirrhosis after transjugular intrahepatic portosystemic shunt. The purpose of this study is to conduct a prospective trial to investigate the incidence of heart failure in cirrhotic patients undergoing transjugular intrahepatic portosystemic shunt ,and to analyze the the predictors and modififications of cardiac function.


Recruitment information / eligibility

Status Recruiting
Enrollment 200
Est. completion date July 2025
Est. primary completion date July 2025
Accepts healthy volunteers No
Gender All
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria: 1. Cirrhosis 2. TIPS is placed successfully 3. Agree to participate in the trial Exclusion Criteria: 1. Non-cirrhotic portal hypertension 2. Previous TIPS or surgical shunt 3. Medium to severe pulmonary hypertension 4. Heart failure 5. End-stage renal disease requiring hemodialysis 6. Respiratory failure 7. Malignancies with a life expectancy of less than 6 months

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
TIPS
TIPS: Established distributary channel between the portal vein and hepatic vein via the jugular vein, portal vein blood directly shunts into the systemic circulation to reduce portal vein pressure to effectively prevent bleeding and refractory ascites.

Locations

Country Name City State
China West China Hospital of Sichuan University Chengdu Sichuan

Sponsors (1)

Lead Sponsor Collaborator
West China Hospital

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Incidence of heart failue Heart failue assessed by2021 ESC Guidelines up to 36 months
Secondary Predictors of heart Failure Heart failue assessed by2021 ESC Guidelines up to 36 months
Secondary mortality Telephone follow-up was performed to collect relevant information up to 36 months
Secondary Modififications of cardiac function Echocardiography was to evaluate cardic function up to 36 months
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