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Acute Kidney Injury clinical trials

View clinical trials related to Acute Kidney Injury.

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NCT ID: NCT01636089 Completed - Clinical trials for Contrast Induced Acute Kidney Injury

Bicarbonates Versus Saline for Contrast Induced Acute Kidney Injury Prevention in Intensive Care Unit

HYDRAREA
Start date: February 2012
Phase: Phase 3
Study type: Interventional

The aim of this study is to compare bicarbonates versus saline for prevention of contrast induced acute kidney injury in critically ill patients.

NCT ID: NCT01625403 Recruiting - Acute Heart Failure Clinical Trials

Recombinant BNP on Heart and Renal Function in Acute Heart Failure

Start date: July 2012
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the efficacy and safety of recombinant human B-type natriuretic peptide (rhBNP) on heart and renal function in patients with acute decompensated heart failure (ADHF) and acute renal injury (AKI).

NCT ID: NCT01621152 Completed - Acute Kidney Injury Clinical Trials

PRevention of Acute Kidney Injury Initiated With Electronic Surveillance Enhancement

PRAISE
Start date: June 2012
Phase: N/A
Study type: Interventional

Introduction: Acute kidney injury (AKI) increases mortality, hospital cost, and rate of progression toward end stage kidney disease 1-4. Early diagnosis and management of AKI is known to improve the above mentioned outcomes. Hypothesis: the investigators will design and validate an electronic surveillance tool to screen all the ICU admissions for the earlier, more efficient diagnosis of AKI and as a result improve the outcome of AKI in ICU patients. Methods: the investigators plan to use the patient database, and AKIN (AKI network) definition to design an electronic alert system to allow clinicians discover patients who develop AKI. Then a randomized clinical trial will be conducted to compare earlier intervention (based on Kidney Disease: Improving Global Outcomes [KDIGO] guidelines) initiated by AKI sniffer alert to the conventional management provided by primary physician in ICU.

NCT ID: NCT01619449 Withdrawn - Clinical trials for Chronic Kidney Disease

Continuous Renal Replacement Therapy in the Setting of Orthotopic Liver Transplant

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

To evaluate the efficacy of continuous renal replacement therapy (CRRT) during orthotopic liver transplantation (OLT) in clearing excess solutes and improving acid-base parameters. The investigators hypothesize that the use of intra-operative CRRT in OLT recipients is associated with increased solute removal and improved acid-base statues when compared to controls who do not receive CRRT

NCT ID: NCT01612013 Completed - Acute Renal Failure Clinical Trials

Intravenous High Dose NAC and Sodium Bicarbonate for the Prevention of Contrast-induced Acute Injury

Start date: May 2005
Phase: N/A
Study type: Interventional

Contrast-induced acute kidney injury is a common cause of acquired in-hospital renal insufficiency and is associated with prolonged hospitalization and unfavorable early and late outcomes. The investigators sought to compare 4 different strategies (intravenous high-dose of N-acetylcysteine, sodium bicarbonate, the combination of both, and saline alone) in the prevention of contrast-induced acute kidney injury in patients undergoing coronary angiography using high-osmolar contrast media defined by creatinine and cystatin C serum levels.

NCT ID: NCT01602328 Terminated - Acute Kidney Injury Clinical Trials

A Study to Evaluate the Safety and Efficacy of AC607 for the Treatment of Kidney Injury in Cardiac Surgery Subjects

ACT-AKI
Start date: June 2012
Phase: Phase 2
Study type: Interventional

Subjects entering the study will have undergone cardiac surgery. Those who experience kidney injury within 48 hours of their surgery will be enrolled into the study. Once enrolled, subjects will receive a single administration of AC607 or placebo. Kidney recovery will be evaluated over the subsequent 30 days and death or the need for dialysis will be evaluated within 90 days of dosing. After 90 days (evaluation period), subjects will enter a 3-year extension phase of the study to monitor safety and long-term outcomes (follow-up period).

NCT ID: NCT01594788 Recruiting - Cardiac Surgery Clinical Trials

Neutrophil Gelatinase-associated Lipocalin as a New Biomarker to Detect Acute Kidney Injury in Postoperative Cardiac Surgery

Start date: April 2011
Phase: N/A
Study type: Observational

Observational study aimed to test the ability of Neutrophil Gelatinase-associated Lipocalin (NGAL) concentration in blood and urine to predict and diagnose early acute renal failure (ARF) in patients after cardiac surgery with/without Cardiopulmonary bypass (CPB).

NCT ID: NCT01594489 Completed - Acute Kidney Injury Clinical Trials

Aminophylline and Contrast Induced Nephropathy in Acute Myocardial Infarction

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

The purpose of this study is to determine whether additional therapy with Aminophylline to hydration with sodium bicarbonate and administration of N-acetylcysteine is more effective to prevent contrast induced acute kidney injury in patients undergoing primary coronary intervention for acute ST elevation myocardial infarction.

NCT ID: NCT01582360 Recruiting - Acute Kidney Injury Clinical Trials

2012_PharmacoCRRT-study:Pharmacokinetics of Anti-infectives in Critically Ill Patients in Need of Continuous Renal Replacement Therapy (CRRT)

PharmacoCRRT
Start date: May 2013
Phase: N/A
Study type: Observational

The main purpose of the study is to examine if changes in pharmacokinetics of important antiinfectives in Critically Ill patients in need of continuous renal replacement therapy (CRRT), causes inadequate concentrations in plasma. The effect of different modus of CRRT: CVVH and CVVHD will be compared, as well as type of filter, filter lifetime etc. Hypothesis: The risk of incorrect dosage of antiinfectives - to low/ to high- is increased in critically ill patients receiving CRRT. Inadequate plasma concentrations of antiinfectives may contribute to increased mortality in this group.

NCT ID: NCT01579396 Withdrawn - Acute Kidney Injury Clinical Trials

High Cut Off Dialysis in Systemic Inflammatory Response Syndrome Patients After Cardiac Surgery

HICOSIRS
Start date: April 2012
Phase: N/A
Study type: Interventional

A high cut off dialyzer (septeX) is tested in patients after cardio-thoracic surgery with incidence of "systemic inflammatory response syndrome" (SIRS) and associated increased risk for acute kidney injury (AKI). Hypothesis: The high cut off dialyzer (septeX) can increase the postoperative IL-6/Il-10 ratio.