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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00755859
Other study ID # IgANSTAZA
Secondary ID
Status Completed
Phase Phase 4
First received September 18, 2008
Last updated September 18, 2008
Start date May 1998
Est. completion date September 2007

Study information

Verified date August 2008
Source A. Manzoni Hospital
Contact n/a
Is FDA regulated No
Health authority Italy: Ethics Committee
Study type Interventional

Clinical Trial Summary

In a previous trial the investigators found that the effect of steroids in IgA nephropathy diminish over time. The difference in renal survival is striking up till the third year, but then remains constant. A six-month course of steroid therapy may be not enough to ensure a stable remission. The investigators hypothesized that a more aggressive treatment may obtain long-term better results. The investigators conducted a randomised controlled trial to assess the utility of low-dose azathioprine added to steroids in adult IgAN patients.


Description:

In 1999, we published a multicenter, randomized, controlled trial, which compared a 6-month steroid course with supportive therapy in 86 patients with IgAN. After 5 years of follow-up, the risk of a 50% increase in plasma creatinine from baseline was significantly lower in the treated patients; proteinuria also decreased. However, the effect of steroids seemed to diminish over time. The difference in renal survival was particularly striking up till the third year, but then remained constant. We hypothesised that a six-month course of steroid therapy is not enough to ensure a stable remission, and a more aggressive treatment may be required to obtain long-term better results. At this regard, some studies of combined treatment with corticosteroids and azathioprine found that treatment was effective in preserving renal function and in reducing proteinuria. However, these studies did not clarify whether azathioprine added further benefit to steroids in the long term. We conducted a randomised controlled trial to assess the utility of low-dose azathioprine added to steroids in adult IgAN patients.


Recruitment information / eligibility

Status Completed
Enrollment 206
Est. completion date September 2007
Est. primary completion date December 2004
Accepts healthy volunteers No
Gender Both
Age group 16 Years to 70 Years
Eligibility Inclusion Criteria:

- biopsy proven IgA nephropathy

- creatinine = 2.0 mg/dl for at least three months

- proteinuria = 1.0 g/day for at least three months

Exclusion Criteria:

- treatment with steroids or cytotoxic drugs during the previous three years

- contraindications to steroids or azathioprine

- Henoch-Schöenlein purpura

- diabetes mellitus

- severe hypertension (diastolic blood pressure > 120 mmHg)

- lupus erythematosus systemicus

- malignancies

- active peptic-ulcer disease

- pregnancy

- viral hepatitis or other infections

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Drug:
steroids plus azathioprine
methylprednisolone 1 g i.v. for three consecutive days at the beginning of months 1, 3 and 5, followed by oral prednisone 0.5 mg/kg every other day plus azathioprine 1.5 mg/kg/day for six months
steroids
methylprednisolone 1 g i.v. for three consecutive days at the beginning of months 1, 3 and 5, followed by oral prednisone 0.5 mg/kg every other day for six months

Locations

Country Name City State
Italy Hospital "S.Marta e S.Venera", Acireale CT
Italy Hospital "Spedali Civili" Brescia
Italy "G. Brotzu" Hospital Cagliari
Italy Hospital "Cannizzaro" Catania
Italy Hospital "Uboldo" Cernusco sul Naviglio MI
Italy Hospital "S.Anna" Como CO
Italy Hospital "Istituti Ospitalieri" Cremona CR
Italy Hospital of Desio Desio MI
Italy Hospital "Careggi" Firenze
Italy Hospital of University Foggia
Italy Department of Nephrology and Dialysis, A. Manzoni Hospital Lecco LC
Italy Hospital "Maggiore" Lodi LO
Italy Hospital "C. Poma" Mantova
Italy Hospital "Maggiore" IRCCS Milano MI
Italy Hospital of Montichiari Montichiari Brescia
Italy Hospital "S. Francesco" Nuoro
Italy Hospital "A.Segni" Ozieri Nuoro
Italy Hospital "V. Cervello" Palermo
Italy University Hospital Parma
Italy Fondazione Maugeri" IRCCS Pavia
Italy CNR-IBIM Reggio Calabria
Italy Hospital "S. Maria Nuova" Reggio Emilia
Italy Hospital "Bolognini" Seriate BG
Italy Hospital of Sondrio Sondrio
Italy Hospital "S.Vincenzo" Taormina CT
Italy CMID Torino
Italy Hospital "Belcolle" Viterbo
Switzerland Inselspital Bern

Sponsors (1)

Lead Sponsor Collaborator
A. Manzoni Hospital

Countries where clinical trial is conducted

Italy,  Switzerland, 

References & Publications (1)

Locatelli F, Pozzi C, Del Vecchio L, Andrulli S, Pani A, Fogazzi G, Altieri P, Ponticelli C. Combined treatment with steroids and azathioprine in IgA nephropathy: design of a prospective randomised multicentre trial. J Nephrol. 1999 Sep-Oct;12(5):308-11. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary progression of renal disease, estimated by the time to 50% increase in plasma creatinine from baseline. Every month for the first six months, then six months Yes
Secondary evolution of proteinuria over time every months for the first six months and then every six months No
Secondary safety every months for the first six months and then every six months Yes
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