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NCT05326399Recruiting

Renal Biopsies in Post-liver Transplantation Patients With Renal Impairment

Renal Biopsies in Post-liver Transplantation Patients With Renal Impairment: a Single-center, Prospective Cohort Study

Source: ClinicalTrials.gov · Last updated 28 Nov 2025

Brief summary (registry, in English)

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.

Status (registry)
Recruiting
Study type
Observational
Enrollment
369 (estimated)
First submitted
26 Mar 2022
Start date
1 Jun 2022
Primary completion date
31 May 2027
Lead sponsor
RenJi Hospital
NCT number
NCT05326399

What you commit to

  • Study type: Observational
  • Planned participants: 369
  • From 1 Jun 2022 to the primary completion date, 31 May 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • patients received renal transplantation

Other illness

  • hepatic failure
  • uncontrolled mental disease or unable to cooperate during operation

Lab values

  • severe bleeding risk or platelet \<70\*109/L
  • chronic kidney insufficiency with eGFR\<30ml/min·1.73m2,or kidney atrophy, or solitary kidney, or medullary sponge kidney, or polycystic kidney, or obstructive nephropathy

Other

  • Pregnancy or lactation
  • not suitable for this study judged by investigaters

Who the study is looking for

  • age 18-75 years
  • patients received liver transplantation
  • new onset of proteinuria(defined as 24-hour proteinuria\>1g/24h, or Urinary albumin creatinine ratio(UACR)\>300mg/g on at least two occasions), and/or renal impairment: eGFR \<60 mL/min/1.73 m² at least two occasions, and/or serum creatinine increase ≥50% from baseline
  • have received renal biopsy in the past 3 months
  • Signed informed consent form(ICF)

Age in the registry: 18 years to 75 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Ren Ji Hospital, Shanghai Jiao Tong University School of Medicine
Coordinator of this site? Confirm its status
ShanghaiChinaNot yet recruiting

This page is information, not medical advice. Discuss any trial with your doctor.