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Renal Insufficiency clinical trials

View clinical trials related to Renal Insufficiency.

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NCT ID: NCT00706771 Completed - Renal Impairment Clinical Trials

Bicarbonate and Lipocalin in Systemic Inflammatory Response Syndrome (SIRS) Study

BLISS
Start date: February 2010
Phase: Phase 2
Study type: Interventional

The investigators will determine the feasibility, safety and efficacy of intravenous sodium bicarbonate in reducing progression to overt acute renal failure in patients with the systemic inflammatory response syndrome, and low urine output or early acute renal impairment as defined by serum neutrophil gelatinase-associated lipocalin (NGAL).

NCT ID: NCT00701714 Terminated - Anemia Clinical Trials

Randomized, Controlled, Double-blind Multicenter Safety Study to Evaluate the Safety and Immunogenicity of Subcutaneous EPO HEXAL vs. ERYPO® in the Treatment of Anemia Associated With Chronic Renal Insufficiency in Predialysis Patients

Start date: September 2007
Phase: Phase 3
Study type: Interventional

This is a randomized, controlled, double-blind, multicenter multinational safety study involving about 300 predialysis patients aged 18 years or above suffering from anemia. Symptomatic anemia will be corrected by s.c. application of EPO HEXAL or ERYPO® in order to achieve a hemoglobin target range of 10.0 -12.0 g/dL.

NCT ID: NCT00700531 Completed - Multiple Myeloma Clinical Trials

European Trial of Free Light Chain Removal by Extended Haemodialysis in Cast Nephropathy

EuLITE
Start date: June 2008
Phase: N/A
Study type: Interventional

Hypothesis: Free light chain removal haemodialysis will increase the rate of renal recovery in patients with cast nephropathy, severe renal failure and de novo multiple myeloma. This study will randomise patients with multiple myeloma and severe renal failure to treatment to remove free light chains by haemodialysis or not.

NCT ID: NCT00696605 Completed - Renal Failure Clinical Trials

Assessment of Circulating Copeptin Levels in Healthy Subjects and Patients With Renal Insufficiency After Oral Water Load and Hypertonic Saline Infusion

Start date: July 2008
Phase: N/A
Study type: Observational

The are 2 principal goals in this study: 1. To measure plasma copeptin levels in healthy subjects and to correlate them with plasma AVP concentrations and urine osmolalities in iso-, hypo-, and hyperosmolar states. 2. To measure plasma copeptin concentrations in patients with chronic renal failure under the same conditions described above, in order to characterize the impact of renal function on circulating copeptin levels in correlation to plasma AVP and urine osmolality.

NCT ID: NCT00695734 Completed - Clinical trials for Chronic Renal Failure

Detection of Latent Tuberculosis in Hemodialysis Patients

Start date: January 2007
Phase: N/A
Study type: Observational

This study aims to compare the performance of the tuberculin skin test, used for more than 50 years as a diagnostic tool for latent tuberculosis infection, with 2 blood tests which have recently become commercially available (Interferon-gamma release assays) in a population of immunosuppressed individuals with chronic renal failure undergoing long term hemodialysis

NCT ID: NCT00694824 Completed - Inflammation Clinical Trials

Vascular Calcification's Risk Factors in Haemodialysis Patients

Start date: November 2004
Phase:
Study type: Observational

A not randomized , cross sectional study will be done to determine the possible association of coronary artery calcification (CAC) score assessed by multirow spiral computed tomography (MSCT) with specific and non specific uremic factor of vascular calcification.

NCT ID: NCT00691756 Completed - Renal Failure Clinical Trials

A Comparison of Renal Perfusion in Thoracoabdominal Aortic Aneurysm (TAAA) Repair

Start date: January 2002
Phase: N/A
Study type: Interventional

The purpose of this randomized trial was to determine whether renal perfusion with cold blood provides better protection against renal ischemia than perfusion with cold crystalloid in patients undergoing TAAA repair with left heart bypass.

NCT ID: NCT00688480 Completed - Kidney Disease Clinical Trials

Do Xanthine Oxidase Inhibitors Reduce Both Left Ventricular Hypertrophy and Endothelial Dysfunction in Cardiovascular Patients With Renal Dysfunction?

Start date: January 2008
Phase: Phase 4
Study type: Interventional

Cardiovascular related disease is the main cause of death in patients with kidney disease, and "oxidative stress" is thought to be a major contributor by promoting thickening of the heart muscle and stiffening of the arteries. Allopurinol, a drug used safely in the treatment of gout for many years, has been found to dramatically reduce "oxidative stress". It is therefore hoped that it also reduce the thickened heart muscle and stiffened arteries. If it did, it is likely to reduce the appallingly high cardiac death rate in this group of kidney disease patients.

NCT ID: NCT00684034 Completed - Clinical trials for Chronic Renal Insufficiency

Redox State in the Course of Chronic Renal Insufficiency and Hemodialysis: Implications in Morbimortality

Start date: June 2008
Phase: N/A
Study type: Interventional

The influence of hemodialysis on oxidative stress, endothelial activation, inflammation and on the redox state of lymphocytes should be clarified as well as the putative relationships between all these parameters.

NCT ID: NCT00683748 Active, not recruiting - Clinical trials for Terminal Liver Failure

Monitoring Cellular Immunity After Kidney and Liver Transplantation

Start date: March 2007
Phase: N/A
Study type: Observational

After transplantation, if insufficient immunosuppression is achieved, rejection and graft loss follows. If to much immunosuppression is given, the patient suffers risk for infections and malignancies. Despite careful dosing and monitoring of drug levels, the biological effects of the immunosuppression given is difficult to predict and varies significantly. As a result, the degree of immunosuppression (or immunosuppressive status) remains unknown and clinical problems related to under- or over-immunosuppression are common. Thus, a method to determine the degree of immunosuppression would be of great and direct clinical importance and the results would be improved. T cells are the principal cells of the immunesystem causing rejection. Furthermore, all immunosuppressive regimes targets T cells. Thus, T cell reactivity could reflect the biological effects of the immunosuppression and the immunosuppressive status. In addition, T cells are of crucial importance in the immunedefence against viral diseases. Therefore, data on virus specific T cell reactivity could aid in diagnosis, monitoring and treatment of viral disease. The proposed study aim to develop a clinically useful method to monitor cellular immunity and the degree of immunosuppression after transplantation by determinations of the specific T cell reactivity to several clinically relevant viruses.