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.