Summary of trial characteristics
Trial | NORAM22 | CYCAZAREM19 | MEPEX20 | CYCLOPS21 | IMPROVE23 | RITUXVAS24 |
---|---|---|---|---|---|---|
Number of patients | 100 | 155 | 137 | 149 | 156 | 44 |
Disease severity | Cr<150 µmol/L, no critical organ disease | Cr<500 µmol/L, no life threatening disease | Cr>500 µmol/L or requiring dialysis | Generalised disease with renal involvement but Cr<500 µmol/L | Any disease severity | Renal involvement |
Treatment | Induction: methotrexate versus cyclophosphamide | Maintenance: cyclophosphamide versus azathioprine | Induction: adjunctive treatment for severe glomerulonephritis | Induction: daily oral versus pulsed cyclophosphamide | Maintenance: mycophenolate mofetil versus azathioprine | Induction: Rituximab versus cyclophosphamide |
Date | 1995–2000 | 1995–2000 | 1995–2002 | 2000–2004 | 2002–2009 | 2006–2007 |
Follow-up | 18 months (treatment for 12 months) | 18 months | 12 months | 18 months | Median of 39 months | 12 months |
LTFU | Yes | Yes | Yes | Yes | No | No |
Cr, creatinine; LTFU, long-term follow-up questionnaire.