Muscle Ultrasound for Sarcopenia Assessment in Kidney Transplant Recipients
Condition(s) studied
Investigational drug(s) / intervention(s)
Muscle Ultrasound: Multimodal muscle ultrasound assessment performed for evaluation of sarcopenia in kidney transplant recipients.
Study summary
This is a single-center prospective observational study designed to evaluate the effectiveness of multimodal muscle ultrasound for the assessment of sarcopenia in kidney transplant recipients. Adult patients undergoing kidney transplantation will undergo both muscle ultrasound and bioelectrical impedance analysis (BIA) at predefined time points before and after transplantation.
The primary objective is to evaluate the diagnostic performance of muscle ultrasound for sarcopenia assessment, including its correlation and agreement with BIA-derived skeletal muscle index (BIA-SMI), as well as its diagnostic accuracy. Secondary objectives include describing the longitudinal changes in sarcopenia prevalence and muscle-related parameters from the pre-transplant period to 1 year after transplantation.
The study aims to provide evidence for a convenient, noninvasive, radiation-free, and reliable method for sarcopenia assessment in kidney transplant recipients.
Eligibility
Primary outcome measure(s)
- Area under the receiver operating characteristic (ROC) curve of muscle ultrasound for detecting sarcopenia using BIA-derived skeletal muscle index (BIA-SMI) as the reference standard. — From baseline to 1 year after kidney transplantation
Diagnostic performance of multimodal muscle ultrasound for sarcopenia assessment using BIA-derived skeletal muscle index (BIA-SMI) as the reference standard, including receiver operating characteristic (ROC) curve analysis and area under the curve (AUC).
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Sichuan Provincial People's Hospital | Chengdu | Sichuan |
More Sichuan Provincial People's Hospital trials in China
Other trials for the same condition
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT07607236 on ClinicalTrials.gov ↗ ← All trials in China