Skip to content

A multicenter, double-blind, randomized controlled clinical trial of Jingtian granule in the treatment of CKD3-5

A multicenter, double-blind, randomized controlled clinical trial of Jingtian granule in the treatment of CKD3-5

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300073249
Enrollment
Unknown
Registered
2023-07-05
Start date
2023-06-20
Completion date
Unknown
Last updated
2023-07-10

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

Conditions

chronic kidney disease

Interventions

Experimental group:Jingtian particles
Control group:placebo

Sponsors

Hubei Provincial Hospital of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: ? Age of 18-75 years old; ? Meet the diagnostic criteria of chronic kidney disease stage 3-5: eGFR < 60 mL/(min*1.73 m2), and is a relatively stable non-dialysis stage; ? Conforming to the TCM diagnostic criteria of deficiency of both qi and Yin and stagnation of water turbidity; ? stable blood pressure below 140/90 mmHg after basic treatment; ?24 h urinary protein = 2.0 g/24 h;

Exclusion criteria

Exclusion criteria: ? Receiving dialysis or hormone, non-steroidal anti-inflammatory drugs, immunosuppressive therapy; ? Severe arrhythmia, acute heart failure, myocardial infarction, acute stroke, unstable angina, NYHA class ? (New York Heart Association classification standard); ? patients with acute infectious diseases, active malignant tumors, active and prolonged chronic hepatitis B, decompensated liver cirrhosis, severe primary diseases such as hematopoietic system, active tuberculosis or mental illness; ? eGFR fluctuation = 30% within 3 months before enrollment; ? serum potassium higher than the upper limit of the reference interval; ? known to be allergic or intolerant to one of the drugs in the study; ? Pregnant or lactating patients; ? Patients who are participating in other clinical studies;

Design outcomes

Primary

MeasureTime frame
Serum creatinine;Glomerular filtration rate;

Secondary

MeasureTime frame
24-hour urinary protein quantification;

Countries

China

Contacts

Public ContactBa Yuanming

Hubei Provincial Hospital of Traditional Chinese Medicine

1723426138@QQ.COM+86 138 7101 3338

Outcome results

None listed

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