One of the most important questions facing nephrology today is whether dietary intervention can arrest or slow down the natural tendency for renal disease to progress to renal failure. The MDRD Trial is designed to answer that question definitively. However, as described in the RFA, to be successful the MDRD Trial must enroll centers which have: 1) The ability to identify and recruity patients who are likely to successfully participate in the Trial; 2) The access to a large patient population, which is geographically stable and medically compliant; 3) The experience to understand the level of commitment needed to successfully execute a study such as this. We respectfully submit that The Ohio State University Renal Division is a center which has the ability, experience, and access to patients which is needed to help make the MDRD Trial Successful. We have been a major participant in the NIH-sponsored Nephrotic Syndrome Trial and the NIH-sponsored Trial of Plasmapheresis in Severe Lupus Glomerulonephritis. We have an ideal patient population, both in size and composition, and a firm committment by the Ohio State University Hospitals and Clinic to provide all of the institutional resources needed to permit us to successfully participate in this trial. Thus, we have carefully analyzed our resources as instructed in the MDRD RFA. That analysis indicates that, if chosen, The Ohio State University Renal Division would be a major contributor to the MDRD Trial.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project--Cooperative Agreements (U01)
Project #
5U01DK039485-06
Application #
3550873
Study Section
Diabetes, Endocrinology and Metabolic Diseases B Subcommittee (DDK)
Project Start
1988-09-30
Project End
1993-11-30
Budget Start
1993-03-15
Budget End
1993-11-30
Support Year
6
Fiscal Year
1993
Total Cost
Indirect Cost
Name
Ohio State University
Department
Type
Schools of Medicine
DUNS #
098987217
City
Columbus
State
OH
Country
United States
Zip Code
43210
Hebert, Lee A; Rovin, Brad H; Hebert, Christopher J (2007) The design of ALLHAT may have biased the study's outcome in favor of the diuretic cohort. Nat Clin Pract Nephrol 3:60-1
Wilmer, William A; Rovin, Brad H; Hebert, Christopher J et al. (2003) Management of glomerular proteinuria: a commentary. J Am Soc Nephrol 14:3217-32
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Hebert, L A; Birmingham, D J; Shen, X P et al. (1994) Rate of antigen entry into the circulation in experimental versus naturally occurring immune complex glomerulonephritis. J Am Soc Nephrol 5:S70-5
Nahman Jr, N S; Maniam, P; Hernandez Jr, R A et al. (1994) Renal artery pressure gradients in patients with angiographic evidence of atherosclerotic renal artery stenosis. Am J Kidney Dis 24:695-9
Hebert, L A; Birmingham, D J; Shen, X P et al. (1992) Stimulating erythropoiesis increases complement receptor expression on primate erythrocytes. Clin Immunol Immunopathol 62:301-6
Hebert, L A; Cosio, F G; Birmingham, D J (1992) The role of the complement system in renal injury. Semin Nephrol 12:408-27

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