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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05040347
Other study ID # QYFYWZLL26511
Secondary ID
Status Completed
Phase
First received
Last updated
Start date August 18, 2020
Est. completion date February 28, 2021

Study information

Verified date September 2021
Source The Affiliated Hospital of Qingdao University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The aim of this study was to investigate whether NETs markers can enhance predict portal vein tumor thrombosis in patients with live cirrhosis, so as to establish a novel predictor to guide clinical decision-making.


Description:

Eighty-six patients with patients treated at the Affiliated Hospital of Qingdao University (China) from September 2020 to January 2021 were recruited for this study, including 14 patients with portal vein tumor thrombosis, 28 patients without portal vein tumor thrombosis and 44 patients without hepatocellular carcinoma. NETs markers (Myeloperoxidase, Neutrophil elastase, Citrate histone H3), and anti-β2 glycoprotein I were detected in plasma using capture ELISA and specific ELISA kits. T-test was performed to analyze whether there was a statistical difference between the two groups, and regression analysis was performed between NETs markers and tissue factor and anti-β2 glycoprotein I to investigate whether there was a correlation. This study without any intervention measures, will not cause harm.


Recruitment information / eligibility

Status Completed
Enrollment 68
Est. completion date February 28, 2021
Est. primary completion date February 28, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria: (1) Clinical diagnosis of HCC with liver cirhosis (2) Clinical diagnosis of portal vein tumor thrombosis Exclusion Criteria: (1) secondary liver malignancy (2)hematologic diseases (3) Bud-Chiah syndrome (4) incomplete data

Study Design


Related Conditions & MeSH terms


Intervention

Other:
test NETs markers
NETs markers (Myeloperoxidase, Neutrophil elastase, Citrate histone H3) and anti-ß2 glycoprotein I were detected in plasma using capture ELISA and specific ELISA kits.

Locations

Country Name City State
China the Affiliated Hospital of Qingdao University Qingdao Shandong

Sponsors (1)

Lead Sponsor Collaborator
The Affiliated Hospital of Qingdao University

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Concentration of NETs markers and anti-ß2 glycoprotein I NETs markers (Myeloperoxidase, Neutrophil elastase, Citrate histone H3) and anti-ß2 glycoprotein I were detected in plasma using capture ELISA and specific ELISA kits. 1 year.
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