Exploring Biomarkers Predicting the Outcome of Acute-on-chronic Liver Failure
NCT ID: NCT02965560
Last Updated: 2018-06-06
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
350 participants
OBSERVATIONAL
2016-10-10
2018-06-01
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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HC,CHB,AD,ACLF
HC healthy controls; CHB chronic hepatitis B; AD acute decompensated cirrhosis; ACLF acute-on-chronic liver failure.
plasma suPAR, PGE2 measurement. Other biomarkers were just recorded from clinical laboratory.
Interventions
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plasma suPAR, PGE2 measurement. Other biomarkers were just recorded from clinical laboratory.
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* Portal vein thrombosis
* Pregnancy
* Human immunodeficiency virus (HIV)
* Patients who had received immunomodulator,or cytotoxic/immunosuppressive therapy within at least the preceding 12 months
18 Years
80 Years
ALL
Yes
Sponsors
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First Affiliated Hospital of Zhejiang University
OTHER
Responsible Party
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Haihong Zhu
Professor
References
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Wang Y, Wu F, Chen C, Xu L, Lin W, Huang C, Yang Y, Wu S, Qi J, Cao H, Li G, Hong M, Zhu H. Soluble urokinase plasminogen activator receptor is associated with short-term mortality and enhanced reactive oxygen species production in acute-on-chronic liver failure. BMC Gastroenterol. 2021 Nov 17;21(1):429. doi: 10.1186/s12876-021-02006-x.
Other Identifiers
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tclouds
Identifier Type: -
Identifier Source: org_study_id
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