Skip to content

Viscoelastic Imaging and Super-Resolution Ultrasound Contrast for Assessing Chronic Kidney Disease Staging: Clinical Study

Viscoelastic Imaging and Super-Resolution Ultrasound Contrast for Assessing Chronic Kidney Disease Staging: Clinical Study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600119567
Enrollment
Unknown
Registered
2026-02-28
Start date
2026-03-01
Completion date
Unknown
Last updated
2026-03-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic kidney disease

Interventions

Gold Standard:1. Glomerular filtration rate (eGFR) below 60 mL/min/1.73 m², persisting for at least three months. 2. Or eGFR is normal but kidney damage persists for at least three months, such as pr
Index test:Super-resolution ultrasound imaging and viscoelastic imaging technology

Sponsors

Peking University Shenzhen Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Age >=18 years; clinically stable and able to cooperate with the ultrasound examination (able to hold breath for a short time/breathing cooperation, can lie flat or on the side); 2. Meets the clinical diagnostic criteria for CKD; 3. Complete routine ultrasound, STVi and SR-CEUS examinations within one week after kidney biopsy; 4. Able to obtain complete baseline data (including but not limited to Scr/eGFR, urinary albumin/proteinuria, blood pressure and main medications); 5. Clinically diagnosed as a CKD patient; 6. Sign the informed consent form, voluntarily participate in the research, and agree to cooperate with the researchers in data collectio.

Exclusion criteria

Exclusion criteria: 1.Those with kidney diseases that severely affect measurement accuracy: multiple renal cysts, multiple kidney stones, renal developmental abnormalities, renal masses, etc. 2. Pregnant and breastfeeding women; 3. Those who are unable to communicate normally and formally sign the informed consent form; 4. Those allergic to contrast agents or with clear contraindications: such as a history of severe contrast agent allergy, severe pulmonary hypertension, inability to cooperate with breath-holding or positioning, affecting image quality, etc; 5. Patients with acute renal failure or acute infectious diseases; 6. Other conditions affecting reproducibility: severe obesity (BMI>37.5 kg/m²) or extremely poor acoustic windows making effective ROI acquisition impossible, subjects deemed unsuitable for enrolment by the researcher, or those unable to complete follow-up.

Design outcomes

Primary

MeasureTime frame
Emean, Vmea, Dmean ;Glomerular filtration rate;Vessel Density, Flow Velocity, FWVD ;ROC curve, ;AUC value ;sensitivity;specificity;

Countries

China

Contacts

Public ContactYixin Zhu

Peking University Shenzhen Hospital

zyx520@pkuszh.com+86 755 8392 3333

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 14, 2026