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Acute Kidney Injury clinical trials

View clinical trials related to Acute Kidney Injury.

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NCT ID: NCT03486184 Not yet recruiting - Clinical trials for Postoperative Acute Kidney Injury

Postoperative Acute Kidney Injury in Patients Undergoing Prolonged Neurosurgical Operations

Start date: May 1, 2018
Phase:
Study type: Observational [Patient Registry]

Postoperative Acute Kidney Injury in Patients Undergoing Prolonged Neurosurgical Operations

NCT ID: NCT03440268 Not yet recruiting - Acute Kidney Injury Clinical Trials

Prevention of Acute Kidney Injury by N-Acetylcystein in Patients Undergone Cardiac Valve Replacement

Start date: March 15, 2018
Phase: Phase 4
Study type: Interventional

This is a randomized clinical trial, double-blind, placebo-controlled study with the goal to assess the influence of using N-AcetylCysteyn (NAC) for prevention of AKI (Acute Kidney Injury) in post operatory of valve replacement until their discharge or death

NCT ID: NCT03369561 Not yet recruiting - Clinical trials for Acute Kidney Injury (Nontraumatic)

Comparison Between Right and Left Ventricular Systolic Dysfunction as a Risk Factors for Aki in Critical Care Patients

Start date: January 1, 2018
Phase: N/A
Study type: Observational

The cardio renal syndrome generally focuses on left ventricular function, and the importance of the right ventricle as a determinant of renal function is described less frequently. Although the risk of AKI is similar for patients with isolated LVD and isolated RVD, the severity of AKI and the associated risk of hospital mortality is highest among those with isolated RVD.

NCT ID: NCT03338127 Not yet recruiting - Acute Kidney Injury Clinical Trials

Outcomes of Acute Kidney Injury in Critically Ill Patients

Start date: December 1, 2017
Phase: N/A
Study type: Observational

this study to evaluate the frequency of acute kidney injury in critically ill patients in intensive care units.

NCT ID: NCT03266367 Not yet recruiting - Acute Kidney Injury Clinical Trials

Neutrophil Gelatinase Associated Liocalin in Predicting AKI in Coronary Artery Disease

Start date: September 15, 2017
Phase: N/A
Study type: Observational

The aim of this work is to assess the clinical significance of serum levels of neutrophil gelatinase-associated lipocalin (NGAL) to predict AKI in patients exposed to PCI.

NCT ID: NCT03206658 Not yet recruiting - Acute Kidney Injury Clinical Trials

Spironolactone on Acute Kidney Injury in Critically Ill Patients

Start date: August 1, 2017
Phase: Phase 3
Study type: Interventional

This study was designed to evaluate the effect of spironolactone administration in the incidence and severity of AKI in patients critically ill with invasive mechanical ventilation (IMV) in the critical care unit. Patients in critical care unit (CCU) are the most at risk of developing AKI. In most cases a mechanism of ischemia/reperfusion has a central role in the development of AKI. Aldosterone has traditionally been recognized as a mediator that maintains water and sodium homeostasis. Nevertheless, there are enough evidence in humans and experimental models that aldosterone might mediate detrimental effects on renal function and structure in pathophysiological conditions. Indeed, several experimental studies from our laboratory have shown that mineralocorticoid receptor blockade protects the kidney against ischemia/reperfusion injury. The aim of this study is to know: o If mineralocorticoid receptor blockade may reduce the incidence and severity of AKI in critically patients with IMV in CCU. You may be able to enter in this study if: - You are at least 18 years old. - You are male or female - You are with IMV. - You are in CCU. - Your serum K is less than 4.5 mEq/L - Your BP is >90/70 mmHg You cannot enter this study if: - You have CKD - You have AKI This study will recruit 90 patients from Instituto Nacional de Ciencias Médicas Salvador Zubiran in México City. The study will begin in April 2017. The patients will be randomized to one of 2 groups of treatment (Spironolactone 25 mg or placebo). All treatments looks identical (1 capsule), will be administered through the nasogastric tube. Neither the patients nor their doctors will be able to know or decide which group you are in. You will receive the medication during the first five days of stay in the critical care unit. As part of this trial, the doctors will ask your permission to get a sample urine during this days. They will use the samples to do tests in the laboratory (different to routine tests) that may help them to compare renal function and biomarkers of renal injury. Your participation will end 10 days after your entry into the critical care unit. The most common side effect of spironolactone is hyperkalemia.

NCT ID: NCT03188614 Not yet recruiting - Shock Clinical Trials

Crystalloids for AKI in Shock Patients

Start date: August 1, 2017
Phase: N/A
Study type: Interventional

Fluid resuscitation is important in shock therapy, but the choice of fluids, especially the choice of crystalloid is under debate. It is said that normal saline is related to hyperchloremia, which might lead to acute kidney injury. Thus the hypothesis of the study is to explicit whether balanced salt solution could reduce the incidence of acute kidney injury when compared with normal saline.

NCT ID: NCT03135483 Not yet recruiting - Clinical trials for Assesse Prevalence of Acute Kidney Injury and Myocardial Injury After Non Cardiac Surgery

Assessment of Acute Kidney Injury as a Risk Factor for Myocardial Injury After Non Cardiac Surgery in Critical Patients

clinical audit
Start date: June 1, 2017
Phase: N/A
Study type: Observational [Patient Registry]

Acute kidney injury (AKI) affects approximately 20% of hospitalized patients and up to 67% of those admitted to an intensive care unit (ICU), making it among the most common organ dysfunctions among the critically ill.Major adverse cardiac events (MACE) after non cardiac surgery are a leading cause of morbidity and mortality. The reported incidence of postoperative myocardial infarction (POMI) among patients undergoing noncardiac surgery is between 3% and 6%.The aim of this study is to Identify the impact of acute kidney injury on the development of myocardial injury after non cardiac surgery and to correlate it with other risk factors of for MINS.

NCT ID: NCT03056248 Not yet recruiting - Acute Kidney Injury Clinical Trials

Lithium in Acute Kidney Injury

LSCAKI
Start date: April 1, 2017
Phase: Phase 4
Study type: Interventional

A growing body of pre-clinical evidence suggests that glycogen synthase kinase 3β (GSKβ) is implicated in the development and progression of acute kidney injury (AKI). Lithium is a naturally occurring standard inhibitor of GSKβ. The purpose of this study is to examined if low dose lithium carbonate is able to reduce the incidence of AKI in patients undergoing cardiac surgery who are placed on cardiopulmonary bypass during surgery. We hypothesize that low dose lithium might reduce the incidence and duration of AKI in patients undergoing cardiac surgery who are on cardiopulmonary bypass.

NCT ID: NCT03034876 Not yet recruiting - Clinical trials for Acute Kidney Injury in Critically Ill Children

Utility of NGAL to Diagnose AKI in Critically Ill Children

Start date: March 1, 2017
Phase: N/A
Study type: Observational

Acute Kidney Injury is common in critically ill children and is associated with high morbidity and mortality in pediatric intensive care unit. The serum creatinine is still a gold standard test for diagnosis of AKI, but it rises after 1 to 3 days of injury . However, Neutrophil Gelatinase-Associated Lipocalcin (NGAL) is an emerging biomarker in identifying AKI at an early stages, which may in future help us in promptly instituting reno-protective interventions like avoidance of nephrotoxic exposure and contrast agents, maintenance of euvolemia and perfusion pressure which will not only preventing kidney from further failing, decrease the use of very expensive and complicated renal supportive therapy like continuous renal replacement therapy (CRRT) as well as in decreasing morbidity and mortality related to AKI.