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Prednisone combined with ARB in the treatment of IgAN with crescentic lesions:A perspective, multi-center randomized controlled trial

Prednisone combined with ARB in the treatment of IgAN with crescentic lesions: a multicenter, randomized, pacebo-controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200064055
Enrollment
Unknown
Registered
2022-09-25
Start date
2022-09-26
Completion date
Unknown
Last updated
2023-04-17

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

Conditions

chronic kidney diseases

Interventions

Group 1:Irbesartan+prednisone

Sponsors

The Second Affiliated Hospital of the Amy Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1.Renal biopsy was pathologically diagnosed as IgAN and the crescent score was C1 (1 = crescent 1.0g/24 hour (or PCR > 1.0g/g) was measured twice in a week.

Exclusion criteria

Exclusion criteria: 1.Secondary IgAN: secondary IgAN caused by systemic diseases such as systemic lupus erythematosus(SLE), congenital purpura and liver cirrhosis. 2.Hepatitis B virus carriers and other chronic liver diseases. 3.All IgAN patients confirmed by biopsies in the study had negative levels of autoimmune antibodies (such as ANA, anti-dsdna, anti-ENA and anti-smith) and were not diagnosed with systemic lupus erythematosus (SLE) according to the guidelines of the American Society of Rheumatology. 4.HIV infection. 5.The patient participates in any other study and has received another research drug or intervention treatment (within the first month before signing the informed consent form). 6.Suspected or known allergy to corticosteroids or irbesartan. 7.Patients who were treated with corticosteroids or irbesartan within the first three months, or with other immunosuppressants or any other biological agents within six months before screening; patients who did not respond to previous immunosuppressants. 8.Women who are positive for pregnancy tests during screening or lactation, or who plan to conceive within 24 months, or who are reluctant to use contraceptive methods throughout the study. 9.Individuals or legal guardians / representatives are unable or unwilling to provide written informed consent. 10.Currently dependent on drug or alcohol use.

Design outcomes

Primary

MeasureTime frame
A 50% drop in eGFR;

Secondary

MeasureTime frame
End-stage renal disease;Urinary protein remission;

Countries

China

Contacts

Public ContactZhao Jinghong

The Second Affiliated Hospital of the Amy Medical University

zhaojh@tmmu.edu.cn+86 13668007369

Outcome results

None listed

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