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Acute Kidney Injury clinical trials

View clinical trials related to Acute Kidney Injury.

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NCT ID: NCT00462527 Completed - Dehydration Clinical Trials

Cystatin C as a Marker for Detecting Early Renal Dysfunction in a Pediatric Emergency Department

CARING
Start date: May 2007
Phase: Phase 1
Study type: Observational

Acute renal failure (ARF) is a rare but serious complication of gastroenteritis and dehydration, the most common reason for pediatric emergency visits. Renal function is determined by the glomerular filtration rate (GFR). Serum creatinine, the current marker of GFR, is insensitive and a late marker of ARF. Unfortunately, "gold standard" methods for measurement of GFR are impractical in the emergency setting. Recently, cystatin C (CysC) was introduced as superior marker for the measurement of GFR, particularly in children. A single random blood sample allows for accurate determination of GFR in the so-called "creatinine-blind" range and independent of the body composition. There is growing evidence that the determination of serum CysC concentration can detect ARF in adults earlier than serum creatinine or urinary fractional sodium excretion. No studies have examined this marker for the early detection of ARF in children at risk. We therefore propose a prospective study that compares CysC with other biomarkers of renal dysfunction for the early detection of ARF in children with dehydration due to gastroenteritis. Patients with minor trauma and a minimal likelihood of ARF will serve as a control. This study may establish CysC as an accurate and cost-effective marker for identifying patients at risk.

NCT ID: NCT00451373 Recruiting - Sepsis Clinical Trials

Acute Renal Failure in the Surgical Intense Care Units - NTUH-SICU-ARF (NSARF) Study

Start date: July 2006
Phase: N/A
Study type: Interventional

We examine the prognosis and etiology of postoperative acute renal failure

NCT ID: NCT00445809 Completed - Clinical trials for Kidney Failure, Acute

Evaluation of Neutrophil Gelatinase-associated Lipocalin (NGAL) in Early and Evolving Acute Kidney Injury

EVOLVE
Start date: February 2007
Phase: N/A
Study type: Observational

Some patients who undergo cardiovascular surgery requiring cardiopulmonary bypass will develop a kidney injury following their surgery. The purpose of this study is to take a blood sample from patients before they have this type of surgery and then at nine time points after their surgery to test their plasma for a biomarker called NGAL and compare the NGAL levels to their creatinine levels. We hypothesize that NGAL is an earlier marker for kidney injury than creatinine.

NCT ID: NCT00424320 Recruiting - Clinical trials for Acute Kidney Failure

Clinical Trial of Sodium Bicarbonate to Prevent Contrast-Induced Nephropathy

Start date: October 2006
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine whether sodium bicarbonate is effective in the prevention of sodium-induced nephropathy

NCT ID: NCT00390624 Completed - Mortality Clinical Trials

Prevention Of Nephrotoxicity Following Bone Marrow Transplantation Using Urodilatin and Mannitol

Start date: July 2003
Phase: Phase 2
Study type: Interventional

The purpose of the study is to combine Urodilatin (ANP analogue), which will increase glomerular filtration rate (GFR), and mannitol, which will increase the rate of urinary flow and solute excretion. We intend to treat twenty consecutive allogeneic bone marrow transplant patients in a phase II study comparing results with historical controls. We hypothesize that the incidence of renal dysfunction, ARF and thus mortality in allogeneic bone marrow transplantation can be significantly reduced by the use of protective agents Urodilatin and mannitol. We feel that this combination is best administered prior to and during the first two weeks of treatment when patients encounter immunosuppressive agents and the onset of early transplantation complications.

NCT ID: NCT00384995 Terminated - Clinical trials for Kidney Failure, Acute

Bicarbonate v Saline to Prevent Contrast Nephropathy

Start date: December 2006
Phase: Phase 4
Study type: Interventional

Slowing of kidney function occurs in a minority of people given dye during angiography. The purpose of this study is to compare two different types of fluid given into a vein to reduce the risk of kidney injury: salt in water or baking soda in water.

NCT ID: NCT00358306 Completed - Clinical trials for Endothelial Dysfunction

The Role of Endothelium Dysfunction in Progression of CKD (Chronic Kidney Disease) After AKI (Acute Kidney Injury)

Start date: April 2008
Phase:
Study type: Observational

To understand how AKI (Acute Kidney Injury) leads to chronic kidney disease so therapies can be found to alter the progression of events thereby significantly impacting the long-term outcomes of children who develop AKI.

NCT ID: NCT00353340 Completed - Clinical trials for Acute Renal Failure Contrast Nephropathy

Prevention of Contrast Nephropathy by Sodium Bicarbonate Versus Sodium Chloride and N-acetylcysteine

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

The objective of this study is to assess the efficacy of sodium bicarbonate compared with sodium chloride and oral N-acetylcysteine (NAC ) pretreatment for prevention of contrast nephropathy in patients with advanced renal disease undergoing cardiac catheterisation.

NCT ID: NCT00337051 Completed - Clinical trials for Renal Transplantation

Renal Transplantation and Inhaled Anesthetic Sevoflurane (SEVOREIN)

SévoRein
Start date: June 2006
Phase: Phase 3
Study type: Interventional

Renal transplantation is characterized by ischemia-reperfusion lesions in allograft. In a previous study, Julier and al. (Anesthesiology 2003) have demonstrated that sevoflurane reduces glomerular lesions in kidney of patients undergoing a cardiovascular surgery and présenting with ischemia-reperfusion phenomena. The purpose of the study is to evaluate the effects of sevoflurane on the recovery of renal graft function in patients after kidney transplantation. This study will be a randomized, double blinded, controlled clinical trial and 120 patients undergoing renal allograft transplantation will be included. Patients will be divided into 2 groups: one group of patients who will receive sevoflurane (evaluated treatment) for anaesthesia and the other one who will receive propofol (reference treatment). We will evaluate renal function for one year after transplantation. Ours results will confirm or not that sevoflurane protects kidney function from ischemia-reperfusion lesions.

NCT ID: NCT00334204 Terminated - Hemorrhage Clinical Trials

Does An Abnormal PFA 100 Predict Bleeding After Renal Biopsy?

Start date: August 2004
Phase: Phase 4
Study type: Interventional

The kidneys are highly vascular organs and any trauma or surgery poses risk of severe bleeding. Platelet function is an integral part of the blood clotting during the initial, so-called vascular phase. So far no universally accepted, easy test has been available to measure platelet functions. Renal failure is a condition generally associated with bleeding due to platelet dysfunctions. This study is exploring the utility of a novel platelet function test, called Platelet Function Analyser-100 to predict bleed after percutaneous kidney biopsy. Platelet Function Analyser-100 will be measure before kidney biopsy along with routine blood tests. Subjects will undergo renal ultrasound before and after renal biopsy to verify post-biopsy bleeding events.