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Acute Kidney Injury clinical trials

View clinical trials related to Acute Kidney Injury.

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NCT ID: NCT02470520 Completed - Clinical trials for Acute Kidney Failure

Essential Nutrients in Critically Ill Patients With Severe AKI Treated With and Without CRRT

Start date: August 2013
Phase: N/A
Study type: Observational

The aim of this study is to measure plasma levels of essential vitamins, trace elements and amino acids in critically ill patients with severe AKI. In patients who are treated with continuous renal replacement therapy, we plan to evaluate whether there are any additional losses of nutrients into the filtrate.

NCT ID: NCT02470507 Active, not recruiting - Clinical trials for Acute Kidney Failure

Immune Function in Acute Kidney Injury

Start date: June 2013
Phase:
Study type: Observational

The immune response to kidney damage during acute kidney injury (AKI) is an important contributor to the prolonged lack of renal function and progression of kidney injury. Most data related to intrarenal and interorgan pathways in AKI stem from animal research with sometimes conflicting results. Accurate evaluation of these processes in humans and identification of early diagnostic tools are critical for the development of strategies to prevent and attenuate AKI-related morbidity and mortality in patients. The aim of this study is to evaluate immune function and miRNA expression in hospitalised patients with and without AKI.

NCT ID: NCT02467075 Terminated - Acute Kidney Injury Clinical Trials

Double-Blind Placebo-Controlled CIN Trial

Start date: July 2015
Phase: Phase 4
Study type: Interventional

This double-blinded placebo-controlled non-inferiority study will examine the incidence and significance of contrast-induced acute kidney injury following intravenous iodinated contrast material administration in subjects with stage IIIB or stage IV chronic kidney disease. Subjects will be scheduled for clinically indicated CT of the abdomen and/or pelvis to evaluate for suspected intra-abdominal infection. Subjects will be randomized to receive either weight-based low-osmolality iodinated contrast material or saline. The primary outcome measure will be the incidence of stage II AKI by AKIN criteria.

NCT ID: NCT02463175 Terminated - Acute Kidney Injury Clinical Trials

Effects of Goal-directed Fluid Therapy on Post-operative Outcomes in Children Undergoing Scoliosis Repair

CardioQ-RP
Start date: June 2015
Phase: N/A
Study type: Interventional

Surgery for scoliosis correction, the abnormal curvature of the spine, is a major procedure often undertaken in adolescents. In adult anesthesia, there is a large volume of literature debating how to optimize fluids administered during surgery, as both too much fluid and too little fluid are associated with worse outcomes. The investigators will compare fluid administration based on the measured amount of blood pumped by the heart during each heart beat (goal-directed therapy), against standard anesthetic management. The main outcomes are a) post-surgical kidney dysfunction, b) prevalence of intraoperative hypotension, c) volumes of administered fluids, and d) length of hospitalization.

NCT ID: NCT02460146 Completed - Acute Kidney Injury Clinical Trials

PK and PD of Sequential Multiple Ascending, Repeat Doses of Oral CXA-10 in Healthy Obese Male Subjects

Start date: April 2015
Phase: Phase 1
Study type: Interventional

The main purpose of this trial is to demonstrate the safety, tolerability and pharmacokinetics (PK) of CXA-10 and its metabolite(s) administered as multiple ascending oral doses over 14 days to healthy obese male volunteers.

NCT ID: NCT02458157 Terminated - Critical Illness Clinical Trials

Forced Fluid Removal in High Risk Acute Kidney Injury

FFAKI
Start date: October 2015
Phase: Phase 4
Study type: Interventional

The objective of this pilot trial is to assess the feasibility of forced fluid removal in patients admitted to the intensive care unit (ICU) with high-risk AKI and severe fluid overload. The intervention will use furosemide infusion and/or continuous renal replacement therapy (CRRT) to achieve and maintain a neutral cumulative fluid balance. The intervention will be compared to standard of care as reflected in the kidney disease improving global outcome (KDIGO) guidelines.

NCT ID: NCT02455115 Completed - Acute Kidney Injury Clinical Trials

Renal Perfusion, Filtration and Oxygenation After Liver Transplantation -Effects of av Postoperative Blood Pressure

Start date: January 2015
Phase: N/A
Study type: Interventional

Comparing the effects of MAP 60, 75 and 90 mmHg, respectively, on renal blood flow, glomerular filtration rate and renal oxygen demand in patients with terminal liver failure directly after liver transplantation.

NCT ID: NCT02453425 Completed - Acute Kidney Injury Clinical Trials

The Effects of Blood Pressure on Renal Function and Oxygenation in Septic Shock

Start date: May 2011
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate renal effects of 3 different levels of mean arterial pressure in early case of septic shock. In 8 patients diagnosed with early septic shock, we will adjust mean arterial pressure (MAP) to three different levels, using norepinephrine. At each level of MAP, central and renal hemodynamics and oxygenation states will be measured. Analysis will be made to describe the pathophysiology at MAP 75 mmHg, and then to evaluate at which MAP renal function and oxygenation is least affected negatively.

NCT ID: NCT02449317 Completed - Clinical trials for X-ray Contrast Media Adverse Reaction

Bioimpedance Analysis Guided Volume Expansion for the Prevention of Contrast Induced-acute Kidney Injury

BELIEVE
Start date: May 2015
Phase: N/A
Study type: Interventional

Bioelectrical impedance analysis guided volume expansion for the prevention of contrast induced-acute kidney injury

NCT ID: NCT02445820 Completed - Clinical trials for Acute Kidney Injury After Adult Cardiac Surgery

HES and Acute Kidney Injury in Adult Cardiac Surgery

Start date: November 2014
Phase: N/A
Study type: Observational

This study retrospectively assess the effect or using balanced hydroxyethyl sctarch (HES) 130/0.4 or a balanced crystalloid solution as a pump prime and for intraoperative fluid therapy on the risk of early acute postoperative kidney injury in adult cardiac surgery patients.