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A randomized controlled trial of mycophenolate mofetil in patients with IgA nephropathy [ISRCTN62574616]
BACKGROUND: IgAN is the most common type of glomerulonephritis in the world. Between 15 and 40 percent of adults and children diagnosed with IgAN eventually progress to ESRD. Despite the need for effective treatment strategies, very few RCTs for IgAN have been performed. The most effective therapies...
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2004
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC415550/ https://www.ncbi.nlm.nih.gov/pubmed/15043759 http://dx.doi.org/10.1186/1471-2369-5-3 |
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author | Hogg, Ronald J Wyatt, Robert J |
author_facet | Hogg, Ronald J Wyatt, Robert J |
author_sort | Hogg, Ronald J |
collection | PubMed |
description | BACKGROUND: IgAN is the most common type of glomerulonephritis in the world. Between 15 and 40 percent of adults and children diagnosed with IgAN eventually progress to ESRD. Despite the need for effective treatment strategies, very few RCTs for IgAN have been performed. The most effective therapies for IgAN appear to be corticosteroids, ACEi, and FOS that contain a high concentration of omega 3 fatty acids. While ACEi and FOS are generally well tolerated with minimal side effects, the use of high dose steroids over a long course of therapy is often associated with significant morbidity. OBJECTIVE OF THE STUDY: The objective of the study is to test the hypothesis that treatment with the immunosuppressive agent, MMF, will lead to significant and sustained improvement in urinary protein excretion in patients with IgAN who have been pre-treated (and continue to be treated) with ACE(i )and FOS compared to a placebo control group of patients receiving comparable doses of ACEi and FOS without MMF. DESIGN: After a three month treatment period with the ACEi, lisinopril and the FOS, Omacor(®), 100 (2 × 50) patients with IgAN and a urinary P/C ratio ≥ 0.6 (males) and ≥ 0.8 (females) and an estGFR ≥ 40 ml/min/1.73 m2 will be randomized to treatment with either MMF or placebo for one year. All patients will be followed off study drug for a second year, but will continue treatment with lisinopril and Omacor(® )for the two year duration of the study. The primary outcome measure of change in urine P/C ratio will be assessed at the end of years one and two. |
format | Text |
id | pubmed-415550 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2004 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-4155502004-05-21 A randomized controlled trial of mycophenolate mofetil in patients with IgA nephropathy [ISRCTN62574616] Hogg, Ronald J Wyatt, Robert J BMC Nephrol Study Protocol BACKGROUND: IgAN is the most common type of glomerulonephritis in the world. Between 15 and 40 percent of adults and children diagnosed with IgAN eventually progress to ESRD. Despite the need for effective treatment strategies, very few RCTs for IgAN have been performed. The most effective therapies for IgAN appear to be corticosteroids, ACEi, and FOS that contain a high concentration of omega 3 fatty acids. While ACEi and FOS are generally well tolerated with minimal side effects, the use of high dose steroids over a long course of therapy is often associated with significant morbidity. OBJECTIVE OF THE STUDY: The objective of the study is to test the hypothesis that treatment with the immunosuppressive agent, MMF, will lead to significant and sustained improvement in urinary protein excretion in patients with IgAN who have been pre-treated (and continue to be treated) with ACE(i )and FOS compared to a placebo control group of patients receiving comparable doses of ACEi and FOS without MMF. DESIGN: After a three month treatment period with the ACEi, lisinopril and the FOS, Omacor(®), 100 (2 × 50) patients with IgAN and a urinary P/C ratio ≥ 0.6 (males) and ≥ 0.8 (females) and an estGFR ≥ 40 ml/min/1.73 m2 will be randomized to treatment with either MMF or placebo for one year. All patients will be followed off study drug for a second year, but will continue treatment with lisinopril and Omacor(® )for the two year duration of the study. The primary outcome measure of change in urine P/C ratio will be assessed at the end of years one and two. BioMed Central 2004-03-25 /pmc/articles/PMC415550/ /pubmed/15043759 http://dx.doi.org/10.1186/1471-2369-5-3 Text en Copyright © 2004 Hogg et al; licensee BioMed Central Ltd. This is an Open Access article: verbatim copying and redistribution of this article are permitted in all media for any purpose, provided this notice is preserved along with the article's original URL. |
spellingShingle | Study Protocol Hogg, Ronald J Wyatt, Robert J A randomized controlled trial of mycophenolate mofetil in patients with IgA nephropathy [ISRCTN62574616] |
title | A randomized controlled trial of mycophenolate mofetil in patients with IgA nephropathy [ISRCTN62574616] |
title_full | A randomized controlled trial of mycophenolate mofetil in patients with IgA nephropathy [ISRCTN62574616] |
title_fullStr | A randomized controlled trial of mycophenolate mofetil in patients with IgA nephropathy [ISRCTN62574616] |
title_full_unstemmed | A randomized controlled trial of mycophenolate mofetil in patients with IgA nephropathy [ISRCTN62574616] |
title_short | A randomized controlled trial of mycophenolate mofetil in patients with IgA nephropathy [ISRCTN62574616] |
title_sort | randomized controlled trial of mycophenolate mofetil in patients with iga nephropathy [isrctn62574616] |
topic | Study Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC415550/ https://www.ncbi.nlm.nih.gov/pubmed/15043759 http://dx.doi.org/10.1186/1471-2369-5-3 |
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