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Clinical Trials/NCT05389280
NCT05389280
Unknown
Not Applicable

Impact of Acute Kidney Injury on Sarcopenia and Frailty in Patients With Liver Cirrhosis

Kangbuk Samsung Hospital1 site in 1 country80 target enrollmentMarch 23, 2022

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Cirrhosis
Sponsor
Kangbuk Samsung Hospital
Enrollment
80
Locations
1
Primary Endpoint
Number of Participants with Acute kidney injury
Last Updated
3 years ago

Overview

Brief Summary

The aim of this prospective observational study is to evaluate the impact of acute kidney injury on sarcopenia and frailty in patients with liver cirrhosis.

Detailed Description

The aim of this prospective study is to collect data on patients with liver cirrhosis and to investigate the impact of acute kidney injury on sarcopenia and frailty in patients with liver cirrhosis. If patients agree to participate in this clinical trial, the patients' data (such as age, sex, height, weight, nutrition status \[RFH-NPT\], history of medication, laboratory findings, endoscopic findings, and radiologic findings) will be collected in a research database. Renal injury was measured using conventional and novel serum biomarkers (serum creatinine, cystatin-C, neutrophil gelatinase-associated lipocalin, kidney injury molecule 1, and interleukin-18. Sarcopenia was evaluated using skeletal muscle index on abdominal computed tomography. Frailty was measured using Liver Frailty Index. The research database will be updated to include data on patients' disease outcomes and follow-up care.

Registry
clinicaltrials.gov
Start Date
March 23, 2022
End Date
March 31, 2023
Last Updated
3 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Kangbuk Samsung Hospital
Responsible Party
Principal Investigator
Principal Investigator

Won Sohn

Principal Investigator

Kangbuk Samsung Hospital

Eligibility Criteria

Inclusion Criteria

  • Liver cirrhosis
  • aged over 20 years

Exclusion Criteria

  • serum creatinine \>1.5 mg/dL
  • on dialysis
  • liver transplant

Outcomes

Primary Outcomes

Number of Participants with Acute kidney injury

Time Frame: up to 24 weeks

an increase in SCr of 0.3 mg/dL (26.4 µmoL/L) in \<48 hours, or a 50% increase in SCr from a baseline within ≤3 months

Study Sites (1)

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