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Clinical Trial Summary

Investigators will conduct this single-center, prospective cohort study to explore the prevalence and risk factors of renal function progression in post-liver transplantation patients with renal impairment after renal biospy and to understand the the pathology of kidney disease in post-liver transplantation patients with renal impairment.


Clinical Trial Description

This is a single-center, prospective, cohort study. This study will include approximate 369 post-liver transplantation patients with renal impairment and have received renal biopsy. Demographic characteristics, medical history, etiology of liver failure, concomitant medications, baseline laboratory parameters, etc., will be recorded. All participants will receive standard treatment by hepatologists and nephrologists based on the pathological results. All participants will be followed up for 96 weeks. Renal function, concomitant medications, and other laboratory parameters, etc., will be obtained. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05326399
Study type Observational
Source RenJi Hospital
Contact Shan Mou, Dr
Phone 13918221242
Email shan_mou@126.com
Status Recruiting
Phase
Start date June 1, 2022
Completion date December 31, 2025

See also
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