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A Clinical Study on the Preliminary Effectiveness of LIPUS Intervention for Diabetic Kidney Disease

A Clinical Study on the Preliminary Effectiveness of LIPUS Intervention for Diabetic Kidney Disease

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500110486
Enrollment
Unknown
Registered
2025-10-14
Start date
2023-11-13
Completion date
Unknown
Last updated
2025-10-20

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

Conditions

diabetic kidney disease

Interventions

Low-intensity pulsed ultrasound treatment group:Low-intensity pulsed ultrasound stimulation

Sponsors

Jiangsu Province Hospital and The First Affiliated Hospital with Nanjing Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Age >=18 years and =9.0%. 3. Estimated glomerular filtration rate (eGFR) calculated using the CKD-EPI formula must be >=30 and =200 mg/g and <=5000 mg/g. 5. Treatment with the maximum tolerated dose of an ACE inhibitor or ARB for at least 4 weeks, with no change in dosage during this period; or not using such treatment due to contraindications. 6. Signed informed consent form.

Exclusion criteria

Exclusion criteria: 1. Active bacterial or viral infection; 2. Pregnant women; 3. Presence of other non-diabetic kidney diseases, such as autosomal dominant/recessive polycystic kidney disease, lupus nephritis, ANCA-associated nephritis, etc. (excluding non-obstructive nephrolithiasis); 4.ALT or AST levels >=3 times the upper limit of normal; 5. Complicated by decompensated liver cirrhosis or hypersplenism; 6. Participants with type 1 diabetes; 7. Use of corticosteroids or immunosuppressants for kidney disease within the past 6 months; 8. NYHA Class IV heart failure within the past 3 months; 9. Newly diagnosed unstable angina or cerebrovascular event within the past 3 months; 10. Blood pressure below 90/60 mmHg or above 180/100 mmHg within the past 2 weeks; 11. Other conditions deemed inappropriate by the investigator, such as clinical instability in overall, metabolic, or cardiovascular health; 12. Participation in other clinical trials within 4 weeks prior to the start of this study.

Design outcomes

Primary

MeasureTime frame
Urine Albumin-to-Creatinine Ratio;24-hour Urinary Protein Excretion;Percentage change in eGFR from baseline;

Secondary

MeasureTime frame
Changes in inflammatory markers;

Countries

China

Contacts

Public ContactHuijuan Mao, Xiangqing Kong

Jiangsu Province Hospital and The First Affiliated Hospital with Nanjing Medical University

maohuijuan72@njmu.edu.cn+86 25 6830 6734

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026