A Multi-center Open Label Prospective Study on Early Initiation of Targeted-release Formulation of Budesonide in Patients With Primary IgA Nephropathy

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-75
SponsorSichuan Provincial People's Hospital

About this trial

To observe of the efficacy and safety of early initiation of budesonide enteric coated capsules in the treatment of primary IgA nephropathy.

Eligibility criteria

Qualifiers

Target patients aged 18-75, including those aged 18 and 75

Primary IgA nephropathy diagnosed by renal biopsy within 3 months

eGFR≥30ml/min/1.73m2

24-hour urine protein ≥ 1.0g/d, or UPCR ≥ 0.8 g/g

Disqualifiers

Including but not limited to secondary IgAN caused by allergic purpura, systemic lupus erythematosus, cirrhosis, rheumatoid arthritis, and ankylosing spondylitis

Patients who have received kidney transplantation or dialysis

Patients with other glomerular diseases (such as C3 glomerular disease and/or diabetes nephropathy) and nephrotic syndrome (i.e. proteinuria>3.5 g/d, serum albumin<3.0 g/dl, with or without edema)

Patients with acute, chronic, or potential infectious diseases, including hepatitis, tuberculosis, human immunodeficiency virus, and chronic urinary tract infections

Trial design

Treatments tested in this trial

  • Gd-IgA1 test

Treatment groups

No treatment groups listed