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Clinical Trial Summary

At present, there is no comparative study between the simple plasma exchange and plasma diafiltration (PDF), and no further exploration of optimal plasma dose in PDF treatment. Therefore, this prospective randomized cohort study aims to compare the safety and effectiveness of the tree groups(simple plasma exchange group, conventional PDF treatment group, less plasma PDF treatment group)by collecting SOFA score, 3-month survival rate, MELD score, and the times of artificial liver treatment , blood cell variables, cytokines(e.g. TNFα ), pre- and post-treatment plasma ammonia levels. Thus, it is to provide a safer and more effective artificial liver treatment with less plasma dose.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03560414
Study type Interventional
Source Fuzhou General Hospital
Contact zhiyu zeng
Phone 008615880447131
Email 498289727@qq.com
Status Not yet recruiting
Phase N/A
Start date June 2018
Completion date December 2020

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