Analysis of Clinical Features of Chronic Liver Disease Complicated With Hepatopulmonary Syndrome
1 other identifier
observational
500
1 country
1
Brief 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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Apr 2023
1 active site
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Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
April 1, 2023
CompletedFirst Submitted
Initial submission to the registry
June 9, 2023
CompletedFirst Posted
Study publicly available on registry
July 6, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 1, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
June 1, 2024
CompletedJuly 6, 2023
July 1, 2023
1 year
June 9, 2023
July 3, 2023
Conditions
Outcome Measures
Primary Outcomes (1)
Proteomic results of participants
Qualitative and quantitative analysis of proteome
April 1,2024
Study Arms (2)
Chronic liver disease with hepatopulmonary syndrome
Liver disease (usually cirrhosis with portal hypertension) ;Positive CE-TTE(Contrast enhanced contrast ultrasound);Abnormal arterial oxygenation: Alveolar-arterial oxygen gradient (AaO2) ≥ 15 mm Hg (\>20 mm Hg if age \> 64)
Chronic liver disease without hepatopulmonary syndrome
Liver disease (usually cirrhosis with portal hypertension) ; Negative CE-TTE
Interventions
Proteomic sequencing, bioinformatics analysis,find abnormal indicators between two groups
Eligibility Criteria
Patients with chronic liver disease admitted to You 'an Hospital.
You may qualify if:
- chronic hepatitis Agreed to venous blood collection
You may not qualify if:
- pneumonia, pulmonary vascular disease, interstitial pulmonary disease, COPD, bronchial asthma, lung cancer and other primary pulmonary diseases, acute upper gastrointestinal bleeding.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Sun Jielead
Study Sites (1)
No.8, Xitoutiao, Youan Men Wai, Fengtai District
Beijing, 100038, China
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- CASE CONTROL
- Time Perspective
- PROSPECTIVE
- Target Duration
- 2 Years
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR INVESTIGATOR
- PI Title
- Professor
Study Record Dates
First Submitted
June 9, 2023
First Posted
July 6, 2023
Study Start
April 1, 2023
Primary Completion
April 1, 2024
Study Completion
June 1, 2024
Last Updated
July 6, 2023
Record last verified: 2023-07