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Diabetic Nephropathy clinical trials

View clinical trials related to Diabetic Nephropathy.

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NCT ID: NCT00317954 Completed - Clinical trials for Diabetic Nephropathy

Spironolactone in Diabetic Nephropathy

Start date: September 2003
Phase: Phase 4
Study type: Interventional

The aim of the study was to evaluate the renoprotective effect (i.e. albuminuria- and bloodpressure lowering effect) of spironolactone 25 mg o.d. in type 1 and type 2 diabetic patients with albuminuria despite recommended antihypertensive treatment.

NCT ID: NCT00315016 Completed - Clinical trials for Diabetic Nephropathy

Eplerenone, ACE Inhibition and Albuminuria

Start date: January 2007
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether eplerenone is more effective than doubling the dose of ACE inhibitor in reducing urinary protein (albumin) loss in diabetes mellitus

NCT ID: NCT00312780 Completed - Clinical trials for Diabetic Nephropathy

Study of XL784 in Patients With Albuminuria Due to Diabetic Nephropathy

Start date: March 2006
Phase: Phase 2
Study type: Interventional

This clinical study is being conducted at multiple sites to determine the activity, safety and tolerability of XL784 when given daily to patients with albuminuria due to diabetic nephropathy. XL784 is a small molecule reno-protective metalloproteinase inhibitor, inhibiting both ADAMs (including ADAM10, a target of significant interest because of its important role in blood vessel formation and cell proliferation, and ADAM17/TACE, activation of which has been associated with renal deterioration) and MMPs (including MMP-2 and MMP-9). XL784 was specifically optimized to be MMP-1 sparing, which may be clinically significant because inhibition of MMP-1 has been hypothesized to be associated with musculoskeletal toxicity.

NCT ID: NCT00311870 Completed - Clinical trials for Diabetic Nephropathy

Renoprotective Effect of Nisoldipine and Lisinopril in Type 1 Diabetic Nephropathy

Start date: March 1993
Phase: Phase 4
Study type: Interventional

The aim of the study was to compare the renoprotective effect of a long acting calcium antagonist (nisoldipine) with an angiotensin converting enzyme inhibitor (lisinopril)in type 1 diabetic patients with diabetic kidney disease. In total, 51 patients were randomised to treatment with one of these drugs for 4 years. Changes in kidney function, blood pressure and urinary excretion of albumin were measured every 6 months

NCT ID: NCT00301249 Completed - Diabetes Clinical Trials

The Family Investigation of Nephropathy and Diabetes Study

FIND
Start date: October 1999
Phase:
Study type: Observational

The Family Investigation of Nephropathy and Diabetes (FIND)Study is a multi-center consortium. The charge of the consortium is to acquire sets of families with well-characterized diabetic nephropathy, establish a secure master FIND database, and perform a genome scan to identify chromosomal regions linked with diabetic nephropathy.

NCT ID: NCT00296296 Completed - Clinical trials for Diabetes Mellitus, Type 2

Immunosuppression Impact on the Metabolic Control of Kidney Transplant With Pre-Existing Type 2 Diabetes (DM)

Start date: June 2005
Phase: Phase 4
Study type: Interventional

Protocol Title: Randomized open label study comparing the metabolic control of first Kidney Transplant recipients with Type 2 Diabetes Mellitus (DM) receiving either Prograf or Neoral as part of a ATG induction, prednisone free and blood monitored Cellcept immunosuppressive regimen. PURPOSE This is a single center medical research study to analyze post-transplant kidney recipients with pre-existing type 2 diabetes managed according to the recommended American Diabetes Association (ADA) guidelines. Prograf (Tac) and Neoral (CSA) are the two main medications to prevent rejection after transplantation. However, they may contribute to poorer diabetes control. The purpose of the study is to compare the effects of Prograf and Neoral on the control of Diabetes after kidney transplantation. In addition, all participants in this study will receive Thymoglobulin (anti-lymphocyte globulin) at the time of transplantation instead of long term prednisone (steroids).

NCT ID: NCT00287183 Completed - Clinical trials for Diabetic Nephropathy

6-Month Safety And Efficacy Study Of TTP488 In Patients With Type 2 Diabetes And Persistent Albuminuria

Start date: February 2006
Phase: Phase 2
Study type: Interventional

Current research indicates that TTP488 may be a viable agent for the treatment of diabetic nephropathy. The purpose of this study is to determine the safety and efficacy of a six-month regimen of daily orally-administered TTP488 to patients with diabetic nephropathy.

NCT ID: NCT00253786 Completed - Clinical trials for Type 2 Diabetes Mellitus

Study for the Effectiveness of Intensive Therapy Aiming at a Remission of Diabetic Nephropathy

Start date: November 11, 2005
Phase: N/A
Study type: Interventional

Study for the effectiveness of intensive therapy aiming at the remission of diabetic nephropathy

NCT ID: NCT00240019 Completed - Clinical trials for Diabetic Nephropathy

Maximizing the Benefit of Renin-Angiotensin Blocking Drugs in Diabetic Renal Disease.

Start date: December 2003
Phase: N/A
Study type: Interventional

The angiotensin converting enzyme inhibitor drugs are now standard therapy for patients with diabetic nephropathy. The hypothesis of this study is that adding a diuretic agent (furosemide) will decrease the urine protein, which is a sign of disease, more than an angiotensin converting enzyme inhibitor alone.

NCT ID: NCT00222846 Completed - Clinical trials for Diabetes Mellitus, Type 2

Enhancing Adherence in Type 2 Diabetes: The ENHANCE Study

ENHANCE
Start date: May 2004
Phase: N/A
Study type: Interventional

This randomized study will test a behavioral intervention, based on social cognitive theory (SCT), to improve regimen adherence in three different groups of people with type 2 diabetes; (1) those with well controlled blood glucoses and no concurrent chronic renal insufficiency, (2) those with less well-controlled glucoses and no chronic renal insufficiency, and (3) those with chronic renal insufficiency regardless of glucose control. The primary aims of this study are to: (1)determine whether the intervention improves behavioral adherence to the diabetes self-management regimen including dietary adherence, physical activity, and capillary glucose self-monitoring; (2)determine whether the intervention improves clinical outcomes; (3) explore the extent to which self-efficacy is a mediator of adherence,(4) explore the extent to which the effectiveness of the intervention varies with respect to glycemic control and nephrovascular complications at baseline, and (5)explore the impact of a variety of covariates on the effectiveness of the intervention. Hypothesis #1 is that intervention group participants will perform better than attention control group participants on various measures of adherence to the diabetes management regimen. Primary adherence variables will be dietary intake, and physical activity. Hypothesis #2 is that intervention group participants will have lower HbA1c levels than attention control group participants.