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Metabolic Acidosis clinical trials

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NCT ID: NCT03035812 Completed - Blood Pressure Clinical Trials

Alkalinization by Urologists & Nephrologists

AlcalUN
Start date: February 1, 2017
Phase: Phase 4
Study type: Interventional

Metabolic acidosis recovers a wide range of diseases in which an oral alkalinization could be useful. This therapeutic intervention has been said to increase extracellular volume leading to rising blood pressure. No prospective data has been published in clinical routine. Here, investigators propose to follow patients in which an oral alkalinization is indicated: blood pressure, body weight, and a clinical evaluation of the extracellular compartment will be performed at the beginning and during the follow-up of participants. The principal criterion of evaluation will be the variation in the extracellular compartment.

NCT ID: NCT02915601 Completed - Clinical trials for Chronic Kidney Disease

Bicarbonate Administration in CKD

Start date: January 15, 2017
Phase: N/A
Study type: Interventional

Low serum bicarbonate levels, even within the normal laboratory range, are strongly associated with increased risks of hypertension, endothelial dysfunction, cardiovascular disease and death. The current proposal will investigate whether bicarbonate administration in patients with chronic kidney disease (CKD) will improve the health and function of arteries and reduce the size of the left ventricle of the heart. Overall, the proposed research will provide important new scientific evidence upon which physicians can base recommendations to patients with CKD to decrease the risk of developing cardiovascular diseases.

NCT ID: NCT02800343 Completed - Metabolic Acidosis Clinical Trials

Intraoperative Cell Salvage and Postoperative Acidosis

Start date: July 8, 2016
Phase:
Study type: Observational

Metabolic acidosis is a common complication that patients experience in the early postoperative period following cardiac surgery. Increasingly, the composition and volume of intravenous fluids administered during surgery have been implicated in the development of postoperative acidosis. Intraoperative Cell Salvage (ICS), an autologous blood transfusion technique employed by Cardiac/Perfusion Units to minimize blood loss during surgery, involves the infusion of of one such fluid, 0.9% sodium chloride. The rapid infusion of large volumes of 0.9% sodium chloride has previously been linked with the development of hyperchloraemic acidosis. It was therefore hypothesized that the volume of mechanically salvaged of red blood cells re-infused into patients undergoing heart surgery contributes to the acidosis that occurs in the early postoperative period. To test this, the investigators have designed an observational cohort study to check for correlation between the volume of cell salvaged blood infused during surgery and the severity of postoperative acidosis (which will be assessed using data from routine arterial blood gas samples).

NCT ID: NCT02476253 Completed - Metabolic Acidosis Clinical Trials

Sodium Bicarbonate to Treat Severe Acidosis in the Critically Ill

(BICAR-ICU)
Start date: May 5, 2015
Phase: Phase 3
Study type: Interventional

The purpose of the present study is to compare the adjunct treatment of metabolic or mixed severe acidosis in the critically ill using Sodium Bicarbonate as a buffer to increase the plasma pH vs no buffering therapy. The study is a randomized multiple center clinical trial with the outcome as a primary endpoint.

NCT ID: NCT02303548 Completed - Cardiac Arrest Clinical Trials

Bicarbonate in Patients With Out-of-hospital Cardiac Arrest

Start date: October 2014
Phase: Phase 2
Study type: Interventional

A pilot study to evaluate the effect of sodium bicarbonate administration on cardiopulmonary resuscitation results and outcomes in cardiac arrest patient with severe metabolic acidosis.

NCT ID: NCT02098356 Completed - Clinical trials for Chronic Kidney Disease

Comparison of High Versus Low Bicarbonate Hemodialysis

Start date: March 2014
Phase: N/A
Study type: Interventional

This study will compare hemodialysis treatment with a standard, high-bicarbonate dialysis bath versus a lower bicarbonate dialysis bath, and will compare intradialytic acid-base changes and overall control of metabolic acidosis with the 2 treatment regimens.

NCT ID: NCT02031770 Completed - Clinical trials for Chronic Kidney Disease

Metabolic Acidosis and Vascular Function in Patients With Chronic Kidney Disease

Start date: January 2014
Phase: N/A
Study type: Interventional

Cardiovascular disease (CVD) is the leading cause of death in patients with chronic kidney disease (CKD) and large artery damage is a major factor that contributes to death. Metabolic acidosis is a common complication of CKD resulting from an inability of the diseased kidney to excrete the daily dietary acid load and it is associated with all-cause mortality in patients with CKD. However, the effect of treatment of metabolic acidosis with oral sodium bicarbonate on endothelial dysfunction and arterial stiffness in patients with CKD has not been evaluated. The investigators propose a prospective, randomized, controlled, open-label 14-week crossover pilot study examining the effect of treatment of metabolic acidosis with oral sodium bicarbonate on vascular endothelial function in 20 patients with CKD stage IV with metabolic acidosis.

NCT ID: NCT01777178 Completed - Clinical trials for Chronic Kidney Disease

Comparison of Standard Versus Low Bicarbonate Hemodialysis

Start date: January 2013
Phase: Phase 1
Study type: Interventional

This study will compare acid-base changes during hemodialysis treatments with a standard dialysis bath versus a lower bicarbonate dialysis bath, and aims to define the factors that limit equilibration of the bicarbonate concentration in a patient's blood with that in the dialysate.

NCT ID: NCT01452412 Completed - Clinical trials for Chronic Kidney Disease

Alkali Therapy in Chronic Kidney Disease

Start date: October 2011
Phase: Phase 2/Phase 3
Study type: Interventional

Kidney disease is a common medical condition. Individuals with kidney disease develop a build-up of acid in their blood. This acid can affect their muscles, bones, glucose metabolism and kidneys. The investigators will test alkali treatment, to treat acid build-up, in a randomized placebo-controlled clinical trial to evaluate effects on muscles, bones, glucose metabolism and kidney.

NCT ID: NCT01295190 Completed - Metabolic Acidosis Clinical Trials

Substitution of Propofol by Sevoflurane During Pediatric Cardiopulmonary Bypass

PRISKIKO
Start date: June 2009
Phase: N/A
Study type: Observational

Propofol has been routinely used for general anesthesia during pediatric cardiopulmonary bypass at our institution without complications. However, propofol may cause propofol infusion syndrome (PRIS), a rare, but often fatal complication mainly defined by bradycardia with progress to asystolia. Metabolic acidosis is regarded as an early warning sign of PRIS. Due to the preconditioning effects of sevoflurane and its availability for cardiopulmonary bypass, propofol has recently been substituted by sevoflurane during pediatric cardiopulmonary bypass at our institution. In this study the effect of substituting propofol by sevoflurane on metabolic acidosis and outcome are examined.