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Efficacy and Safety of the Chinese Herbal Formula Granules in Chronic Kidney Disease Stage 3: A Prospective, Multi-center, Randomized, Placebo-controlled, Double-blind Clinical Trial

Efficacy and Safety of the Chinese Herbal Formula Granules in Chronic Kidney Disease Stage 3: A Prospective, Multi-center, Randomized, Placebo-controlled, Double-blind Clinical Trial

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900026000
Enrollment
Unknown
Registered
2019-09-17
Start date
2016-01-01
Completion date
Unknown
Last updated
2019-09-30

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

Conditions

Nephrology

Interventions

Sponsors

Affiliated Hospital of Nanjing University of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: Male and female patients diagnosed as primary CKD aged 18-75 years with estimated glomerular filtration rate (eGFR) >= 30 ml/min/1.73m2 and < 60 ml/min/1.73m2 calculated with the Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI) equation and 24-hour proteinuria <=2.0 g/d. Blood pressure was managed <=130/80 mmHg.

Exclusion criteria

Exclusion criteria: Patients with acute kidney injury, polycystic kidney disease, secondary kidney disease such as diabetic nephropathy were not recruited. Patients were receiving glucocorticoids, immunosuppressants and Tripterygium drug were excluded. Patients with concurrent serious disease, including primary cardiac, cerebral, pulmonary, hepatic, hematological, psychiatric disease, and pregnancy or lactation were also not included.

Design outcomes

Primary

MeasureTime frame
24-hour Proteinuria;Serum Creatinine;Serum Creatine;eGFR;Urea Nitrogen;blood routine examination;Adverse Events;

Countries

China

Contacts

Public ContactWei Sun

Department of Nephrology, Affiliated Hospital of Nanjing University of Chinese Medicine

kqwonr@126.com+86 14763482294

Outcome results

None listed

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