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Acute Renal Failure clinical trials

View clinical trials related to Acute Renal Failure.

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NCT ID: NCT00892359 Recruiting - Infection Clinical Trials

Anidulafungin During Continuous Venovenous Hemofiltration (CVVHF)

Start date: April 2009
Phase: Phase 2
Study type: Interventional

The purpose of this trial is to study the pharmacokinetics of anidulafungin during continuous venovenous hemofiltration. Background: Anidulafungin is a cyclic lipopeptide antifungal agent of the echinocandin class. Members of this class of antifungal agents are known to inhibit the synthesis of glucan polymers in fungal cell walls. The spectrum of activity of anidulafungin includes Candida (all species, including strains resistant to fluconazole), Aspergillus, and Pneumocystis. In intensive care patients continuous venovenous haemodiafiltration (CVVHF) is a well-established extracorporal renal replacement therapy with a high clearance rate. Pharmacokinetic studies of antifungal agents in critically ill patients treated with CVVHF are rare. No data about anidulafungin in CVVHF are available although intensive care patients are perfect candidates for anidulafungin treatment due to their high risk profile for systemic fungal infections. Study objective: The study is conducted to investigate the pharmacokinetics of anidulafungin during CVVHF in critically ill patients. Study design: open, 1 arm Study population: 10 critically ill adult patients administered to the ICU with acute renal failure and suspected or proven fungal infection. Treatment/Dosage/Route: On the first day 200 mg of anidulafungin will be administered intravenously over 3 hours (loading dose). The following days 100 mg of anidulafungin will be administered intravenously over 1.5 hours. Main outcome variables: The following pharmacokinetic parameters will be determined: area under the curve (AUC), half-live (t1/2), maximum plasma concentration (Cmax) and elimination fraction. Methods: High pressure liquid chromatography (HPLC) will be used to determine anidulafungin concentrations.

NCT ID: NCT00875069 Completed - Infection Clinical Trials

Efficacy and Safety of Ethanol Lock Solution in Prevention of Catheter Related Bloodstream Infection for Patients Suffering Acute Renal Failure, and Hospitalized in Intensive Care Unit. A Multi-Center, Randomized, Versus Placebo, Double Blinded Clinical Trial

ELVIS
Start date: April 2009
Phase: Phase 3
Study type: Interventional

The primary objective of the study is to demonstrate the efficacy of 60% ethanol lock solution in preventing major catheter related infections in critically ill patients.

NCT ID: NCT00870883 Completed - Hypotension Clinical Trials

N-acetylcysteine Plus Deferoxamine for Patients With Hypotension

Start date: March 2009
Phase: Phase 2
Study type: Interventional

Oxidative stress is associated with kidney damage in several different situations, including hypotension. In animal models it has been shown that the combination of n-acetylcysteine plus deferoxamine is superior to its isolate use in the treatment of several diseases. Thus the investigators aimed to determine if the administration of n-acetylcysteine plus deferoxamine could prevent renal failure in critical ill patients who develops hypotension.

NCT ID: NCT00851851 Completed - Clinical trials for Chronic Renal Failure

New Non-invasive Methods for Real-time Monitoring of Organ Function.

RTMKF
Start date: January 2009
Phase: N/A
Study type: Observational

Measuring novel proteins in the urine of surgical patients that can be used to diagnose impending acute or chronic renal failure.

NCT ID: NCT00816790 Terminated - Septic Shock Clinical Trials

Standard Vs Adjusted Dosing of Piperacillin/Tazobactam in Acute Renal Failure and Septic Shock

Start date: January 2009
Phase: Phase 4
Study type: Interventional

The objective of this study is to determine the feasibility of conducting a large scale randomized controlled trial comparing standard and renally adjusted dosage of antibiotics in the septic shock patients with acute renal dysfunction. We will use Piperacillin as the prototype antibiotic in our study.

NCT ID: NCT00791648 Completed - Acute Kidney Injury Clinical Trials

Short-term Atorvastatin's Effect on Acute Kidney Injury Following Cardiac Surgery

Start date: July 2009
Phase: N/A
Study type: Interventional

Aim1a: Statin naive patient's scheduled for cardiac surgery will be randomized to 80mg atorvastatin or placebo on the day prior to surgery and then 40mg daily thereafter until hospital discharge to test the hypothesis that short-term atorvastatin use decreases: 1. acute kidney injury following cardiac surgery. 2. postoperative delirium following cardiac surgery. Aim1b: Patients using statins preoperatively will be randomized to atorvastatin 80mg or placebo on day of surgery and 40mg or placebo on postop day 1 with resumption of preoperative statin therapy on postop day 2 to test the hypothesis that short-term atorvastatin use decreases: 1. acute kidney injury following cardiac surgery. 2. postoperative delirium following cardiac surgery. Endpoints include glomerular filtration, urine and plasma markers of renal dysfunction, markers of oxidative stress, mitochondrial function, systemic inflammatory markers, delirium, dialysis, stroke, myocardial infarction, time to extubation, ICU length of stay, and death.

NCT ID: NCT00780351 Completed - Acute Renal Failure Clinical Trials

Dosing Vancomycin in Patients on Sustained Low Efficiency Daily Hemodiafiltration (SLEDD-f)

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

1. Sustained low efficiency daily hemodiafiltration(SLEDD-f) is a kind of renal replacement therapy with high-flux dialyser membrane (helixone). 2. The pore size of helixone is larger than most antibiotics, and vancomycin is supposed to be removed during dialysis. 3. Our study wants to find the amount of vancomycin removed during SLEDD-f, and try to find the most appropriate dose regimen for this kind of patients.

NCT ID: NCT00752453 Completed - Acute Renal Failure Clinical Trials

Uremic Toxins in the Intensive Care Units (ICU): Patients With Lactate Acidosis

Start date: July 31, 2008
Phase: N/A
Study type: Interventional

Study of the kinetics of uremic toxins in the ICU patients with acute renal failure, in order to optimize the dialysis dose: patients with lactate acidosis. The sampling of blood and dialysate will be done during dialysis with different durations (4, 6 and 8 h)

NCT ID: NCT00743132 Completed - Acute Renal Failure Clinical Trials

Novel Prediction Score for Postoperative Acute Renal Failure (ARF) Following Liver Resection

StV 11-2008
Start date: April 2008
Phase: N/A
Study type: Observational

ARF is a frequent event after hepatic resection and therefore clinically highly relevant. There is limited evidence on the incidence of postoperative ARF and its clinical relevance in patients undergoing liver resection. This study will evaluate the incidence of acute renal failure (ARF) after liver resection and its impact on postoperative mortality.

NCT ID: NCT00736827 Completed - Sepsis Clinical Trials

BK Virus and Renal Dysfunction in Postoperative/Posttraumatic Critically Ill Patients

BICUK
Start date: August 2008
Phase: N/A
Study type: Observational

The purpose of this study is to find out whether acute renal failure is associated with BK virus reactivation in postoperative/posttraumatic critically ill patients with severe SIRS/sepsis and shock.