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Fluid Overload clinical trials

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NCT ID: NCT04215692 Recruiting - Fluid Overload Clinical Trials

Lung Ultrasound-guided Fluid Therapy in Pediatric Intensive Care Unit Patients

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

A randomized clinical trial to evaluate the effect of using pulmonary ultrasound to guide fluid therapy on distinct variables.

NCT ID: NCT04198168 Terminated - Acute Kidney Injury Clinical Trials

The Predictive Performance of Renal Ultrasound on Changes in Renal Clearance

Start date: January 1, 2020
Phase:
Study type: Observational

The study will examine the ability of renal ultrasound (Doppler and Contrast Enhanced Ultrasound (CEUS)) in distinguishing ICU patients who exhibit increases in glomerular filtration rate (GFR) in response to fluid loading, from those for whom fluid loading is without benefit of directly harmful.

NCT ID: NCT04194047 Completed - Anemia Clinical Trials

Effects of Red Blood Cells Transfusion on Renal Blood Flow

Start date: March 1, 2020
Phase:
Study type: Observational

The renal Doppler resistive index (RRI) is a noninvasive tool that has been used to assess renal perfusion in the intensive care unit (ICU) setting. It is associated with the occurrence of acute kidney injury (AKI). Many parameters have been described as influential on the values of renal RI. Red blood cell (RBC) transfusion were shown to be able to increase renal oxygenation in animal model, whereas crystalloid resuscitation did not. We sought to describe the different effect of crystalloids infusion and RBC transfusion on renal blood flow, as evaluated with doppler ultrasound

NCT ID: NCT04180397 Recruiting - Fluid Overload Clinical Trials

Controlled Fluid Removal in Critical Ill Patients With Fluid Overload in the Intensive Care Unit.

GODIF
Start date: August 17, 2020
Phase: Phase 4
Study type: Interventional

This study evaluates the benefits and harms of goal directed fluid removal with furosemide versus placebo in critical ill adult patients with fluid overload in the intensive care unit. Half of the patients will receive furosemide and the other half placebo. The treatment will continue until the excess fluid is excreted.

NCT ID: NCT04151160 Completed - Clinical trials for Congenital Heart Disease

Point of Care Ultrasound Measurements of Perioperative Edema in Infants With Congenital Heart Disease

Start date: January 13, 2020
Phase:
Study type: Observational

Babies can be born with heart problems and sometimes need a heart surgery to fix the heart problem. Heart surgery can cause swelling from the build-up of extra fluid. Swelling can make it harder for babies to breath and has to be treated with medicine called diuretics. Swelling is hard to measure in babies, so it can be hard to know how much diuretic they need to treat the swelling. The investigators are looking for a better way to measure swelling in babies who have had heart surgery. Ultrasound uses sound waves to take pictures of the inside of the body. Ultrasound is used to take pictures of babies before they are born and to take pictures of their heart after they are born. New ultrasound software has been made from a company called MuscleSound that can quickly measure the amount of swelling in adults, usually in less than 2 minutes. This software has not yet been used to measure swelling in kids. This study plans to learn more about swelling in babies and will try to measure swelling in babies before and after heart surgery with the new ultrasound software. The study will also make the same measurements in babies who do not have heart disease to compare to babies having heart surgery.

NCT ID: NCT04095143 Completed - Acute Kidney Injury Clinical Trials

Ultrasound Markers of Organ Congestion in Severe Acute Kidney Injury

ECHO-AKI
Start date: September 4, 2018
Phase:
Study type: Observational

Fluid overload is associated with adverse outcomes in patients with severe acute kidney injury. It remains unclear if fluid overload is merely a marker of disease severity or if organ congestion is a mediator of complications. Point-of-care ultrasound could be a modality used to assess organ congestion and its clinical implications. The objective of this study is to determine whether ultrasound markers of organ congestion are associated with major adverse kidney events in critically ill patients with severe acute kidney injury.

NCT ID: NCT03997721 Completed - Fluid Overload Clinical Trials

Pathophysiology of Perioperative Fluid Management in Emergency Laparotomy

Start date: May 23, 2019
Phase:
Study type: Observational [Patient Registry]

Pathophysiology of perioperative fluid management in patients undergoing emergency laparotomy.

NCT ID: NCT03974906 Completed - Clinical trials for Postoperative Complications

Goal-directed Fluid Therapy in Elderly Patients Undergoing Lumbar Surgery

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

This is a randomized controlled clinical trial which investigates whether goal directed fluid therapy( GDT ) would show the evidence of benefit from GDT in terms of lactate kinetics then may reduce postoperative complications in patients undergoing spine surgery, especially in prone positions.

NCT ID: NCT03972475 Completed - Critical Care Clinical Trials

The Effect of Maintenance Fluids on Overall Fluid Balance in ICU Patients

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

The amount of fluids characterized as non-resuscitation fluids given to ICU patients are likely to be high and will probably have a substantial impact on the total amount of fluid administered to ICU patients daily. It will most likely also influence on the total fluid balance and the negative outcome of fluid overload. The aim of our study is to investigate the amount of fluid given as maintenance fluids in the ICU and the impact of this fluid on total fluid balance.

NCT ID: NCT03956901 Completed - Fluid Overload Clinical Trials

Goal Directed Fluid Management , Pvi

Start date: April 8, 2019
Phase: N/A
Study type: Interventional

The first objective of this study is to compare the liberal fluid management (LFM) with PVI guided goal-directed fluid management (GDFM) in gynecologic oncologic cases in terms of controlled intraoperative fluid balance, blood lactate levels, hemodynamic parameters, and postoperative serum creatinine levels. 112 patients who are in ASA I-II-lll risk groups included in this prospective study.