- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05909319
Identification and Verification of Neutrophil Extracellular Trap Net Related Markers in Acute-on-chronic Liver Failure
June 11, 2023 updated by: First Affiliated Hospital of Wenzhou Medical University
Acute-on-chronic liver failure (ACLF) refers to the acute deterioration of liver function in patients with chronic liver disease.
Neutrophils are a major component of the innate immune system, and previous studies have revealed enhanced production of neutrophil extracellular traps (NETs) in ACLF.
However, there is still a lack of systematic research on the correlation between NETs and the prognosis of ACLF.
We screened NETs related biomarkers through bioinformatics analysis, which play an important role in the diagnosis of ACLF.
This study will explore whether these NETs related biomarkers also play an important role in the prognosis of ACLF and further investigate their role in the pathogenesis of ACLF.
Study Overview
Status
Not yet recruiting
Conditions
Study Type
Observational
Enrollment (Estimated)
200
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Sampling Method
Probability Sample
Study Population
Patients who meet the diagnostic criteria of Chinese Group on the Study of Severe Hepatitis B (COSSH) for acute-on-chronic liver failure
Description
Inclusion Criteria:
1. Patients who meet the diagnostic criteria of Chinese Group on the Study of Severe Hepatitis B (COSSH) for acute-on-chronic liver failure
Exclusion Criteria:
- Age greater than 75 years old
- liver cancer
- previous liver transplantation
- other serious extrahepatic organ diseases
- uncontrolled bacterial infections.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
|---|
|
ACLF
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
mortality
Time Frame: 30 days
|
mortality of patients with ACLF
|
30 days
|
|
mortality
Time Frame: 90 days
|
mortality of patients with ACLF
|
90 days
|
|
mortality
Time Frame: half a year
|
mortality of patients with ACLF
|
half a year
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Estimated)
June 25, 2023
Primary Completion (Estimated)
December 25, 2024
Study Completion (Estimated)
June 25, 2025
Study Registration Dates
First Submitted
May 29, 2023
First Submitted That Met QC Criteria
June 11, 2023
First Posted (Estimated)
June 19, 2023
Study Record Updates
Last Update Posted (Estimated)
June 19, 2023
Last Update Submitted That Met QC Criteria
June 11, 2023
Last Verified
April 1, 2023
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2023-3-14 version V1.0
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.