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Renal Insufficiency clinical trials

View clinical trials related to Renal Insufficiency.

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NCT ID: NCT01560572 Completed - Clinical trials for Kidney Transplantation

Steroid Free Immunosuppression or Calcineurin Inhibitor Minimization After Basiliximab Induction Therapy in Kidney Transplantation: Comparison With a Standard Quadruple Immunosuppressive Regimen

Allegro
Start date: April 2011
Phase: Phase 4
Study type: Interventional

A prospective, open, randomized trial, in which the investigators aim to achieve optimal immunosuppression after renal renal transplantation with maximal reduction of side effects, especially of vascular injury, chronic allograft nephropathy, osteoporosis and malignancies. Immunosuppression without steroids and CNI minimization is compared to standard immunosuppression, consisting of tacrolimus OD, mycophenolic acid and corticosteroids.

NCT ID: NCT01558323 Completed - Renal Impairment Clinical Trials

Pharmacokinetics of LCQ908 in Patients With Renal Impairment

Start date: May 2012
Phase: Phase 1
Study type: Interventional

This study will compare the pharmacokinetics of LCQ908 in subjects with varying degrees of renal impairment to healthy subjects

NCT ID: NCT01555866 Completed - Healthy Volunteers Clinical Trials

Study of the Effect of Renal Impairment on the Pharmacokinetics of Isavuconazole.

Start date: March 2012
Phase: Phase 1
Study type: Interventional

This is a 2-part, open-label study, designed to evaluate the effect of renal disease on the pharmacokinetics of BAL4815 (active isavuconazole moiety) relative to the pharmacokinetics in healthy subjects with normal renal function.

NCT ID: NCT01555008 Completed - Clinical trials for Type 2 Diabetes Mellitus

Study to Evaluate the Pharmacodynamic and Pharmacokinetic Effects of LX4211 in Subjects With Type 2 Diabetes and Renal Impairment

Start date: March 2012
Phase: Phase 1
Study type: Interventional

This Phase 1 study is intended to assess the pharmacodynamics (PD), pharmacokinetics (PK), safety and tolerability of LX4211 following once daily oral administration in subjects with type 2 diabetes mellitus (T2DM) and moderate to severe renal impairment.

NCT ID: NCT01554982 Completed - Clinical trials for End Stage Renal Disease

A Long-Term Safety Extension Trial of Ferric Citrate in Patients With End-Stage Renal Disease (ESRD) on Dialysis

Start date: August 2012
Phase: Phase 3
Study type: Interventional

A long-term safety study of ferric citrate (KRX-0502) in renal failure patients who have completed study KRX-0502-304. Only patients who participated in the KRX-0502-304 trial may participate in this trial.

NCT ID: NCT01545531 Completed - Renal Insufficiency Clinical Trials

Two-Point Measurement of Glomerular Filtration Rate by Iohexol Plasma Disappearance

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

The purpose of this study is to measure glomerular filtration rate (GFR) by iohexol plasma disappearance (gold standard) and measure serum Cystatin C levels (surrogate marker) in patients enrolled in our prospective study at baseline, day 100 and 1 year after hematopoietic cell transplant and determine if these levels correlate with serum creatinine and an estimated GFR using the Modification of Diet in Renal Disease (MDRD) equation and Schwartz formula in children.

NCT ID: NCT01544231 Completed - Clinical trials for Acute Kidney Failure

Plasma Neutrophil Gelatinase Associated Lipocalin Levels During Emergency Management of Rhabdomyolysis

Start date: August 2013
Phase: N/A
Study type: Observational

This research project consists of a prospective diagnostic study conducted on patients with clinical suspicion of rhabdomyolysis admitted to the emergency rooms of the University Hospitals of Nimes, Montpellier, Paris, Nice and Toulon Inter Army Hospital. The main objective of this study is to determine whether the plasma level of Neutrophil Gelatinase Associated Lipocalin (NGAL) may be retained as a predictor of acute renal failure (ARF) occurring within 48 hours after admission for rhabdomyolysis.

NCT ID: NCT01537757 Completed - Alzheimer's Disease Clinical Trials

A Two-Part, Single-Dose Study of the Pharmacokinetics of MK-8931 in Subjects With Renal Insufficiency (MK-8931-009 [P08535])

Start date: March 2012
Phase: Phase 1
Study type: Interventional

This study will assess the pharmacokinetics of MK-8931, a ß-secretase inhibitor, in participants with renal insufficiency. In Part 1 of the study, pharmacokinetics of MK-8931 in participants with severe renal disease and in healthy matched control participants will be studied. If data from Part 1 confirms that severe renal impairment does not alter the pharmacokinetics of MK-8931 to the extent requiring dosage adjustment, then no further study will be required and Part 2 will be optional. If the data does not support this conclusion, then Part 2 will be conducted to study the pharmacokinetics of MK-8931 in participants with moderate and mild renal impairment compared to healthy matched controls.

NCT ID: NCT01536548 Completed - Clinical trials for Chronic Kidney Disease

Indicating Direction and Angle for Cannulating of AV-fistula in Hemodialysis Patients

Start date: March 2012
Phase: N/A
Study type: Interventional

Arteriovenous fistula is the preferred access for hemodialysis, and cannulation using a "button-hole" technique is increasingly recommended. By using the same two sites for cannulation there are reports of less risk of complications and less pain for the patient. However, button-hole cannulation can be difficult for the dialysis nurse, and failing cannulations can damage the AV fistula and increase patient discomfort. The investigators therefore will test whether a simple marking on the skin of the direction and angle of cannulation used in each specific patient could improve the probability of a successful and painfree cannulation.

NCT ID: NCT01534364 Completed - Acute Renal Failure Clinical Trials

Brief Title:Effect of a Preoperative Calorie Restriction on Renal Function After Cardiac Surgery

CR_KCH
Start date: January 2012
Phase: N/A
Study type: Interventional

The aim of this study is to assess the effect of a diet prior to cardiac surgery on the common postoperative decline of renal function. Until now, there is no known drug or procedure to preserve the kidneys from this impairment. Patients with a known kidney disease are especially at risk. A potential beneficial effect of a diet prior to surgery has been shown in investigations in mammals, therefore this study will investigate if a preoperative diet in patients with known kidney disease and scheduled heart surgery can attenuate or prevent a postoperative loss of kidney function.