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dc.contributor.authorClarke W.R.en
dc.contributor.authorHunsicker L.G.en
dc.contributor.authorRodby R.A.en
dc.contributor.authorRohde R.D.en
dc.contributor.authorLewis E.J.en
dc.contributor.authorRitz E.en
dc.contributor.authorAtkins R.C.en
dc.contributor.authorAnzalone D.A.en
dc.date.accessioned2021-05-14T11:16:38Zen
dc.date.available2021-05-14T11:16:38Zen
dc.date.copyright2000en
dc.date.created20000403en
dc.date.issued2012-10-19en
dc.identifier.citationNephrology Dialysis Transplantation. 15 (4) (pp 487-497), 2000. Date of Publication: 2000.en
dc.identifier.issn0931-0509en
dc.identifier.urihttps://repository.monashhealth.org/monashhealthjspui/handle/1/33254en
dc.description.abstractBackground. Diabetic nephropathy is the most common cause of end-stage renal disease in the developed world. Angiotensin-converting enzyme inhibitors have been demonstrated to be renoprotective in type I diabetes and are now the standard of care for both hypertensive and non-hypertensive type I diabetic patients with any level of proteinuria. The role of blockade of the renin-angiotensin system in type II diabetic patients is not defined. The Collaborative Study Group has initiated the Irbesartan Type II Diabetic Nephropathy Trial (IDNT), studying the effect of the angiotensin II receptor antagonist irbesartan on progression of renal disease and mortality in type II diabetic patients with overt nephropathy and hypertension. Here we report the study design and baseline patient characteristics. Methods. To qualify, hypertensive type II patients, age 30-70 years, must have a 24 h urinary protein excretion of > 900 mg and a serum creatinine 90-265 mumol/l (1.0-3.0 mg/dl) in women and 110-265 mumol/l (1.2-3.0 mg/dl) in men. Three treatment arms include irbesartan, placebo and amlodipine, with every attempt made to achieve similar blood pressure levels in all treatment arms. A total of 1650 patients will be enrolled utilizing ~225 clinics worldwide. The primary outcome measure is time to event to the composite end-point of doubling of serum creatinine, end-stage renal disease or death. The secondary outcome measure is time to composite end-point of fatal or non-fatal cardiovascular events. The average length of patient follow-up is expected to be ~36 months. Results. The baseline characteristics of the study subjects are: age 59 +/- 8 years, duration of diabetes 15 +/- 9 years, height 168 +/- 11 cm (5 ft 6 in), weight 87 +/- 19 kg (192 lb), body mass index 31 +/- 7 kg/m2, blood pressure 156 +/- 18 mmHg/85 +/- 11 mmHg, serum creatinine 150 +/- 53 mumol/l (1.7 +/- 0.6 mg/dl), creatinine clearance 66 +/- 34 ml/min and 24 h urine protein 4.0 +/- 3.5 g/day.en
dc.languageEnglishen
dc.languageenen
dc.publisherOxford University Press (Great Clarendon Street, Oxford OX2 6DP, United Kingdom)en
dc.titleThe irbesartan type II diabetic nephropathy trial: Study design and baseline patient characteristics.en
dc.typeArticleen
dc.type.studyortrialRandomised controlled trial-
dc.identifier.doihttp://monash.idm.oclc.org/login?url=http://dx.doi.org/10.1093/ndt/15.4.487en
dc.publisher.placeUnited Kingdomen
dc.identifier.pubmedid10727543 [http://www.ncbi.nlm.nih.gov/pubmed/?term=10727543]en
dc.identifier.source30160655en
dc.identifier.institution(Rodby, Rohde, Lewis) Section of Nephrology, Department of Medicine, Rush Medical College, Chicago, IL, United States (Clarke, Hunsicker) Division of Biostatistics, Department of Preventive Medicine, University of Iowa, Iowa City, IA, United States (Anzalone) Bristol Myers Squibb P., Princeton, NJ, United States (Atkins) Monash Medical Centre, Clayton, Vic., Australia (Ritz) University of Heidelberg, Heidelberg, Germany (Rodby) Rush-Presbyt. St. Luke's Med. Center, 1653 W. Congress Parkway, Chicago, IL 60612, United Statesen
dc.description.addressR.A. Rodby, Rush-Presbyterian St Lukes Med. Ctr., 1653 W. Congress Parkway, Chicago, IL 60612, United Statesen
dc.description.publicationstatusEmbaseen
dc.rights.statementCopyright 2012 Elsevier B.V., All rights reserved.en
dc.subect.keywordsAngiotensin II receptor antagonist Diabetic nephropathy Renoprotection Type II diabetesen
item.fulltextNo Fulltext-
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.grantfulltextnone-
item.openairetypeArticle-
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