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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05932927
Other study ID # 2022-096
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date April 1, 2023
Est. completion date June 1, 2024

Study information

Verified date July 2023
Source Beijing YouAn Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

Hepatopulmonary syndrome (HPS) has unknown pathogenesis, limited treatment and poor prognosis. The onset of HPS is insidious and easy to be ignored. Many liver diseases such as "cirrhosis and related complications" are the core characteristics of Beijing You 'an Hospital, but the clinical characteristics of HPS patients in the center are still unclear. The investigators plan to make the diagnosis of HPS among chronic liver disease patients in the hospital according to the diagnostic criteria of HPS proposed in the Practice Guidelines of the International Society of Liver Transplantation in 2016, collect clinical data of HPS participants, evaluate the severity, analyze and summarize clinical characteristics, and conduct management and follow-up. At the same time, The investigators collect blood samples for proteomics tests. In order to improve the diagnosis and treatment level of HPS.


Description:

At present, the mechanism of hepatopulmonary syndrome is not clear. The researchers plan to use the extracted plasma for detection, protein extraction and quality control, and then proteolytic hydrolysis, computer detection, and bioinformatics analysis.


Recruitment information / eligibility

Status Recruiting
Enrollment 500
Est. completion date June 1, 2024
Est. primary completion date April 1, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years to 100 Years
Eligibility Inclusion Criteria: - chronic hepatitis Agreed to venous blood collection Exclusion Criteria: - pneumonia, pulmonary vascular disease, interstitial pulmonary disease, COPD, bronchial asthma, lung cancer and other primary pulmonary diseases, acute upper gastrointestinal bleeding.

Study Design


Intervention

Biological:
Proteomic sequencing
Proteomic sequencing, bioinformatics analysis,find abnormal indicators between two groups

Locations

Country Name City State
China No.8, Xitoutiao, Youan Men Wai, Fengtai District Beijing

Sponsors (1)

Lead Sponsor Collaborator
Sun Jie

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Proteomic results of participants Qualitative and quantitative analysis of proteome April 1,2024
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