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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT04976764
Other study ID # QYFYWZLL26462
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date August 1, 2021
Est. completion date September 1, 2023

Study information

Verified date July 2021
Source The Affiliated Hospital of Qingdao University
Contact shenghua Bi
Phone +8618863608195
Email bsh112359@163.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Liver transplantation is an effective treatment for end-stage liver disease. Cardiovascular complications are the common causes of death in liver transplant recipients. The presence of cirrhosis cardiomyopathy has a potential impact on the prognosis of liver transplant recipients. Therefore, it is important to identify the high risk factors with cirrhotic cardiomyopathy before transplantation, so as to intervene earlier and improve the prognosis of patients.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 850
Est. completion date September 1, 2023
Est. primary completion date August 1, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria: 1. Diagnostic criteria for decompensated liver cirrhosis: according to the guidelines for diagnosis and treatment of liver cirrhosis in 2019; 2. Diagnostic criteria for cirrhotic cardiomyopathy: in accordance with the revised criteria of CCM of international multidisciplinary Alliance for cirrhotic cardiomyopathy in 2019, the preoperative echocardiographic images of all patients were reviewed, and the systolic and diastolic dysfunction of all patients were evaluated. Exclusion Criteria: 1. the compensatory liver cirrhosis, primary liver cancer without liver cirrhosis 2. Multiple organ transplantation or multiple organ transplantation 3. The preoperative echocardiographic data were not fully recorded, so that the exact diagnosis could not be made 4. There was no follow-up data or baseline data

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
The Affiliated Hospital of Qingdao University

Outcome

Type Measure Description Time frame Safety issue
Primary perioperative cardiovascular events there are differences between 2 groups. 2012.1.1-2022.8
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