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Acute Renal Injury clinical trials

View clinical trials related to Acute Renal Injury.

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NCT ID: NCT04600271 Completed - Acute Renal Injury Clinical Trials

Acute Renal Injury After Major Elective Non-Cardiac Surgery

Start date: June 1, 2019
Phase:
Study type: Observational

The study is planned to be a single-center study and includes patients who underwent major surgery within Istanbul University Istanbul Faculty of Medicine with an invasive arterial line. Our aim to define the incidence of acute renal injury in our setting and to investigate the risk factors listed in detailed description. After obtaining written informed consent from the patients, preoperative risk factors will be notes. Following standard anesthesia monitoring as well as routine anesthesia induction and maintenance, invasive arterial monitoring will be performed due to the major surgery and hemodynamic values will be recorded throughout the surgery. The primary outcome will be acute renal injury based on KDIGO's (Kidney Disease: Improving Global Outcomes) definition of acute renal damage. Postoperative data regarding this outcome as well as additional data listed in detailed description will be collected.

NCT ID: NCT02974946 Completed - Acute Renal Injury Clinical Trials

Kidney Protection Using the RenalGuard® System in Cardiac Surgery

KIDNEY
Start date: January 2017
Phase: N/A
Study type: Interventional

This is a prospective randomised control trial 1:1 in patients at risk of developing Acute Kidney Injury after cardiac surgery comparing the RenalGuard® System to current medical treatment. 110 patients will be recruited for each group. The aim of the study is to assess whether the RenalGuard® system reduces Acute Kidney Injury (AKI) after cardiac surgery as compared to current practice.

NCT ID: NCT02838667 Completed - Acute Renal Injury Clinical Trials

Prevention and Early Detection and Intervention of Post-Coronary Artery Bypass Grafting Surgery (CABG) Acute Kidney Injury (AKI)

Start date: July 1, 2016
Phase: N/A
Study type: Interventional

Nephrology participation in care of patients undergoing CABG could reduce AKI through correction of modifiable risk factors and early detection and intervention of post-op AKI.

NCT ID: NCT02765464 Completed - Acute Renal Injury Clinical Trials

Acute Kidney Injury in Critically Ill Patients

Start date: October 1, 2016
Phase:
Study type: Observational

Acute kidney injury (AKI) in critically ill trauma patients has been shown to significantly increase mortality, length of stay, and costs, however detection has proven difficult as markers like elevated creatinine and decreased urine output may take days to manifest and are late indicators of AKI. The combination of two urinary biomarkers, Tissue Inhibitor of Metalloproteinase 2 (TIMP-2) and Insulin-like Growth Factor Binding Protein 7 (IGFBP-7), has been shown to increase within 12 hours following renal insult, allowing assessment of risk for developing acute kidney injury. Therefore, the investigators plan to assess if acute kidney injury in critically ill trauma patients can be determined earlier using urinary TIMP-2 and IGFBP-7 via the NephroCheck testing system. These markers have not been specifically evaluated in trauma patients at risk of AKI.

NCT ID: NCT01920542 Completed - Acute Renal Injury Clinical Trials

Dexmedetomidine on Pediatric Heart Operation

Start date: September 2013
Phase: N/A
Study type: Interventional

we hypothized dexmedetomidine could reduce the reduction of renal function after cardiopulmonary bypass weaning in pediatric patients

NCT ID: NCT01807195 Completed - Acute Renal Injury Clinical Trials

Acute Renal Injury Associated Contrast in Intensive Care Unit Patients

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

Generally, a contrast medium is used when performing a CT scan or radiographic tests such as angiography because it heightens image clarity and can increase diagnosis accuracy. Despite these advantages, contrast media can cause allergic reactions in the body or a decline in renal function. Therefore, they should be handled carefully and explained sufficiently to the patient. For intensive care patients, the use of contrast agents has been revealed as a major cause of acute renal damage, and many studies have investigated this complication by examining incidence rates and prevention strategies. Hypothesis: Among intensive care patients, the group in which a contrast medium was used will have a higher risk of renal function decline compared with the group in which a contrast medium was not used, and, hence, the use of contrast media becomes a cause of renal function deterioration. Categorizing patients with renal function decline according to the new RIFLE criteria can have an association with the prognosis of intensive care patients, such as hospitalization period and death rate, which can promote faster intervention.