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Therapeutic effect and safety of Huangkui Capsule for chronic kidney disease: a multi-center, randomized, open label study

Therapeutic effect and safety of Huangkui Capsule for chronic kidney disease: a multi-center, randomized, open label study

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-10000923
Enrollment
Unknown
Registered
2010-07-05
Start date
2010-07-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

chronic kidney disease

Interventions

A:Huangkui Capsule, 2.5g, tid,for 24 weeks
B:Losartan, 50mg qd, for 24 weeks
C:Huangkui Capsule, 2.5g, tid+ losartan 50mg qd, for 24 weeks

Sponsors

Chinese General Hospital of PLA
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1.Renal biopsy proven primary glomeruli disease in 1 year; 2. Age range 18-70 years, male and female; 3. BP=60ml/min; 5. Proteinuria levels of 0.5 to 2.0g/24hr; 6. Signed the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Secondary glomeruli disease such as lupus nephritis, Henoch-Schonlein purpura nephritis, glomerulonephritis due to systemic small vessel vasculitis, diabetic nephropathy, hypertensive nephropathy, gouty nephropathy, myeloma kidney, et al; 2. The participants used the same treatment of traditional Chinese medicine or ACEI/ARB in the previous 4 weeks; 3. Received steroids/immunosuppressive drugs/Radix Tripterygii Wilfordii treatment for more than 3 months, and showed a poor clinical response; 4. With severe diseases in heart, brain, liver, kidney or hematopoietic system,as well as other diseases which seriously affected life ; 5. Pregnant or breast-feeding women; 6. Allergy history of Abelmoschus Manihot or losartan; 7. With poor compliance; 8. Participate in other clinical trials meanwhile; 9. Any other conditions that researchers think not suitable for this experiment.

Design outcomes

Primary

MeasureTime frame
24 hour urinary protein excretion;

Secondary

MeasureTime frame
Level of serum cretinine, eGFR, serum albumin, CRP;

Countries

China

Contacts

Public ContactXiangmei Chen
xmchen301@126.com+86 10 66935462

Outcome results

None listed

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