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AKI clinical trials

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NCT ID: NCT04266834 Completed - Clinical trials for Contrast-induced Nephropathy

Establishing Clinical Utility of a New Diagnostic Test in Patients Undergoing Cardiac Catheterization

Start date: December 1, 2019
Phase: N/A
Study type: Interventional

This study will collect high-quality randomized controlled data across the U.S. from practicing cardiologists performing invasive/interventional procedures and determine how they currently manage patients at risk for CIN and how the results of Hikari's L-FABP test change clinical decision making.

NCT ID: NCT04112953 Completed - AKI Clinical Trials

Intraoperative Transesophageal Echocardiography Assessment of Portal Vein Flow and Renal Resistive Index As a Predictor of Acute Kidney Injury After Cardiac Surgery: A Prospective Observational Study

Start date: September 4, 2019
Phase:
Study type: Observational

The purpose of this study is to better understand if transesophageal echocardiography during cardiac surgery can predict problems with kidney function after cardiac surgery.

NCT ID: NCT04048525 Completed - Sepsis Clinical Trials

Cytokine Removal With CVVHD Compared to CVVH

Start date: March 13, 2013
Phase: N/A
Study type: Interventional

Septic patients with acute kidney injury (SA-AKI) requiring continuous renal replacement therapies (CRRT) present high mortality due to systemic inflammatory response, cytokine liberation, and finally multiorgan dysfunction. Cytokine plasmatic elimination with continuous venovenous hemofiltration (CVVH) presents a high resource cost both technical and human. The study primary end-point is to demonstrate a similar cytokine removal of continuous venovenous hemodialysis (CVVHD) respect to CVVH, both modalities employing the same adsorption capacity membrane. As secondary end-points investigators will try to demonstrate technical superiority of CVVHD respect to CVVH. In order to achieve these objectives investigators have designed a proof of concept exploratory trial that will include those participants whom present SA-AKI meeting CRRT initiation criteria. During the first 72 hours investigators will measure plasmatic elimination capacity of main cytokines, and other clinical and prognostic relevant molecules. Investigators wil measure mean filter life during all CRRT with special attention to the first 72 hours. Investigators will also measure hemodynamic, respiratory, and metabolic parameters. Finally, investigators will analyze 90 days survival. Demonstration of a similar immunomodulating capacity and a minor complication rate with its consequent lower cost, should settle the based evidence principles that recommend the use of CVVHD associated to an adsorption capacity membrane in patients with SA-AKI whom need CRRT.

NCT ID: NCT03740425 Completed - Clinical trials for Aortic Valve Stenosis

Transfusion Requirements in Transcatheter Aortic Valve Implantation (TRITAVI) Study

TRITAVI
Start date: January 1, 2018
Phase:
Study type: Observational

Periprocedural bleeding events are frequent during transcatheter aortic valve implantation (TAVI), mainly driven by vascular complications and are associated to a worse prognosis. Therefore, red blood cell (RBC) transfusion is often required, although it is associated with worsened outcomes. There is no consensus on the optimal transfusion strategy after bleeding. The Transfusion Requirements in Transcatheter Aortic Valve Implantation (TRITAVI) will be a multicenter retrospective registry enrolling consecutive patients who underwent TAVI; the primary aim of the study will be to test whether RBC transfusion is a marker or an independent predictor of adverse events.

NCT ID: NCT03591536 Completed - Inflammation Clinical Trials

Effects of Pentoxifylline After Cardiac Surgery

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

Acute Kidney Injury (AKI) is a common and serious post operative complication and may occur in up to 50% of all patients undergoing cardiac surgery and is associated with 8% mortality rate compared with 0.9% in non-affected patients and remains a major factor for post surgery adverse outcomes. Early interventions to prevent postoperative AKI can help decreasing morbidity and mortality in these patients. Using cardiopulmonary bypass during cardiac surgery triggers systemic inflammatory response and recruits pro-inflammatory cytokines such as tumor necrosis factor, interleukin -10 (IL-10) and Interleukin-6 (IL-6) accompanying with production of free oxygen radicals which provokes oxidative stress in the milieu of ischemic reperfusion injury. Pentoxifylline as a non-specific phosphodiesterase inhibitor, can suppress the production of some factors of inflammatory response and oxidative stress, probably prevent post surgery AKI with these mechanisms.

NCT ID: NCT03391830 Completed - Clinical trials for Contrast-induced Nephropathy

Effects Of Combination Therapy Of Statin And Ascorbic Acid For Prevention Of Contrast-Induced Nephropathy

Start date: January 15, 2018
Phase: N/A
Study type: Interventional

To evaluate the benefit for statin use in prevention of of CI-AKI after computed tomography urogram (CTU).

NCT ID: NCT03070353 Completed - Cirrhosis, Liver Clinical Trials

Dextran, a Plasma Expander, Offers New Hope for Patients With Decompensated Liver Cirrhosis and Acute Kidney Injury

Start date: July 1, 2015
Phase: Phase 2/Phase 3
Study type: Interventional

A pilot study of Dextran-40 infusion in patients with decompensated cirrhosis presenting with AKI