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Prospective trial of leflunomide in the treatment of immunoglobulin A nephropathy

Prospective trial of leflunomide in the treatment of immunoglobulin A nephropathy

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IPR-14005368
Enrollment
Unknown
Registered
2014-09-24
Start date
2014-11-01
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

immunoglobulin A nephropathy

Interventions

Experimental group:leflunomide 20mg/d

Sponsors

West China Hospital of Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1.Aged between 18 to 65 years; 2. 24 hrs proteinuria of more than 1.0g, but less than 3.0 g; 3.CKD stage range from 1 to 3; 4. No steroid or immunosuppressor used before.

Exclusion criteria

Exclusion criteria: 1. Secondary IgA nephropathy such as Henoch-Schonlein purpura, ankylosing spondylitis, psoriatic arthritiswith spondyloarthropathy, chronic alcoholic cirrhosis; 2. Combine with other kidney injury: Diabetic Nephropathy, obesity related glomerulopathy, interstitial nephritis and so on; 3. obvious liver dysfunction (transaminase three times above normal) or the abnormal of coagulation, lower WBC (less than 2*10^9); 4. pregnancy or Lactation; 5. Drug sensitivity or drug allergy.

Design outcomes

Primary

MeasureTime frame
24-h proteinuria;urine red blood cells;glomerular filtration rate;serum creatinine;blood urea nitrogen;

Secondary

MeasureTime frame
WBC;liver function;serum albumin;

Countries

China

Contacts

Public ContactLI ZI
lizihx@163.com+86 18980601212

Outcome results

None listed

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