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Acute Kidney Injury clinical trials

View clinical trials related to Acute Kidney Injury.

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NCT ID: NCT01573962 Completed - Acute Kidney Injury Clinical Trials

A Sample Collection Study to Validate the Astute Medical NephroCheck Test in Critically Ill Subjects at Risk for Acute Kidney Injury

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

The objective of this sample collection study is to collect blood and urine samples. This study is observational and will have no impact on the medical management of the subject.

NCT ID: NCT01573104 Completed - Acute Kidney Injury Clinical Trials

Evaluating Novel Biomarkers in Acute Kidney Injury

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

The investigators have a new technique of looking at urine to see whether it contains protein fragments that are released by damaged kidneys. These fragments seem to be more accurate than the current blood tests that the investigators use to diagnose renal failure. This technique needs to be validated with a group of patients that have a relatively high incidence of renal failure, cardiopulmonary bypass. The investigators hypothesise that using novel markers of renal dysfunction will identify patients who go on to develop renal failure earlier, and in a higher number than the standard blood tests. The investigators aim to collect urine from patients before going onto bypass, and then at Day 1 and Day 2 after bypass. This urine will be analysed for protein fragments, as well as other new markers of renal dysfunction. The investigators will also take blood at baseline and for the first two days in Cardiac Intensive Care, and compare the accuracy of the new tests with the 'gold standard' that is creatinine.

NCT ID: NCT01569698 Terminated - Clinical trials for Kidney Failure, Acute

Modalities of Renal Replacement Therapy in Pediatric Acute Kidney Injury

EPURE
Start date: June 2012
Phase:
Study type: Observational

Limited prospective data is available to compare morbidity and mortality between renal replacement modalities in pediatric acute renal failure. In the absence of clear standard of care, the choice of the extra renal replacement therapy modality is subject to clinical judgement, practical aspects, and costs. This study will supply important data about usual modalities of pediatric acute extra renal replacement therapy and their impact on patient outcome and renal recovery. An obvious next step will be to conduct a randomized controlled trial comparing the different strategies.

NCT ID: NCT01562925 Completed - Clinical trials for Contrast-medium Induced Acute Kidney Injury

Effect of Red Wine, White Wine and Beer on Contrast-Medium Induced Acute Kidney Injury

RenPro-II-WINE
Start date: March 2012
Phase: Phase 3
Study type: Interventional

Patients with impaired renal function are at elevated risk for development of contrast-medium induced acute kidney injury (CI-AKI). CI-AKI is associated with increased risk for cardiovascular morbidity and mortality. Effective CI-AKI prevention strategies are needed. The RenPro-II-WINE Trial was designed to test the hypothesis whether moderate red wine consumption prior to contrast-medium use is effective in CI-AKI prevention. Consecutive patients with impaired renal function undergoing elective coronary angiography will be assigned in one of four treatment arms: a. control patients receiving standard care b. patients receiving standard care plus red wine c. patients receiving standard care plus white wine d. patients receiving standard care plus beer This study will give important answers on how to prevent CI-AKI in patients with impaired renal function undergoing contrast media exposure.

NCT ID: NCT01561885 Completed - Asthma Clinical Trials

Collaborative Healthcare Professionals Approach in Monitoring of Patient Centered Outcomes Through Pathways

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

The aim of this study is to determine if by providing a collaborative, integrated pathway-based healthcare compared to the usual healthcare, whether or not this would be superior in reducing the length of hospital stay across five high frequency /high risk medical diagnoses: Acute Venous Thromboembolism, Acute Kidney Injury, Community Acquired Pneumonia, Adult Left Ventricular Heart Failure, and Asthma.

NCT ID: NCT01560650 Completed - Acute Kidney Injury Clinical Trials

Effect of the Intensity of Continuous Renal Replacement Therapy in Patients With Acute Kidney Injury

Start date: March 2011
Phase: Phase 4
Study type: Interventional

The current international Continuous Renal Replacement Therapy (CRRT) replacement fluid doses of 35 ml/kg/h is better, but the result is according to white people, black people . It is Whether the best amount of replacement fluid for Chinese people, it is unclear. Especially,there is little evidence about the optimal dose from randomized trials in Cardiac surgery associated acute kidney injury (CSA-AKI )required CRRT,According to the clinical situation, the design of replacement fluid to 25 ml/kg/h.The observation of two doses 14 days, 28 days, 90 days survival and renal function.

NCT ID: NCT01557361 Completed - Acute Kidney Injury Clinical Trials

Standard Versus Accelerated Initiation of Dialysis in Acute Kidney Injury

STARRT-AKI
Start date: May 2012
Phase: Phase 2
Study type: Interventional

The objectives of this trial are to determine whether, in critically ill patients with severe acute kidney injury (AKI), randomization to accelerated initiation of renal replacement therapy (RRT), compared with standard initiation, is: 1. Feasible, in terms of adherence to the protocol (primary outcome), recruitment rates, and achievement of follow-up; and 2. Safe, from the perspective of potential adverse events associated with earlier initiation of RRT

NCT ID: NCT01554345 Recruiting - Acute Kidney Injury Clinical Trials

Effect of Vitamin E+Selenium on Kidney Function in Controlled Hypotension

Start date: June 2011
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether Kidney injury happens in controlled hypotension during brain operations by using Neutrophil Gelatinase Associated Lipocalin ELISA Kit and if so, does VitaminE+Selenium prevent it

NCT ID: NCT01552525 Completed - Acute Kidney Injury Clinical Trials

L-Arginine, Symmetrical and Asymmetrical Dimethylarginine (SDMA/ADMA) in Acute Kidney Injury (AKI)

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

The purpose of the study is to determine the association between acute kidney injury and serum levels symmetrical and asymmetrical dimethylarginine (SDMA/ADMA) and their assumptive influence on mortality, renal function and on arterial stiffness.

NCT ID: NCT01547455 Completed - Acute Kidney Injury Clinical Trials

Safety and Efficiency Study of Loading Dose Atorvastatin in Cardiac Surgery

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

Statins were reported to have pleiotropic effects including antiinflammatory, anti-oxidative stress effects and stabilise plaque in some conditions. Some researches indicate loading dose statin can reduce contrast induced nephropathy, and the levels of inflammatory markers were significantly decreased. The investigators hypothesis loading dose atorvastatin may attenuate inflammatory response during cardiopulmonary bypass (CPB) and therefore reduce postoperative acute kidney injury in cardiac surgery.