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Metabolic Acidosis clinical trials

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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: NCT01894594 Terminated - Clinical trials for Chronic Kidney Disease

Efficacy, Safety Study and Benefit of Alkali Therapy in Sickle Cell Disease

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

The objective of this study is to assess the effect of alkali administration on bicarbonate and potassium levels in patients with Sickle Cell Disease (SCD) and depressed serum bicarbonate levels. The study is a prospective non-blinded evaluation of tolerability and efficacy of alkali repletion with 4 weeks of observation and two sequential 4 week courses of escalating oral sodium bicarbonate treatment.

NCT ID: NCT01860001 Recruiting - Metabolic Acidosis Clinical Trials

Incidence of Postoperative Ketosis and Metabolic Acidosis

POKACID
Start date: October 2012
Phase: N/A
Study type: Observational

The aim of this study is to define the incidence and nature of acidosis after major surgery using Figge's equations to directly measure acidosis. This study will also aim to compare the ability of indirect measures (base deficit, anion gap,corrected anion gap and lactate) to identify the presence of tissue acids in this population. The incidence of postoperative ketoacidosis as a contributor to tissue acidosis will be assessed through the use of point of care urinalysis.

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: NCT01640119 Recruiting - Metabolic Acidosis Clinical Trials

Correction of Metabolic Acidosis in End Stage Renal Disease (ESRD)

UBI
Start date: July 2014
Phase: Phase 3
Study type: Interventional

The investigators want to evaluate whether an original action based on the administration of alkali (mainly sodium bicarbonate) is able to significantly modify renal death and to reduce mortality due to cardiovascular events. Methods: This is a proposal of Multicentric, prospective, cohort, randomized, open-label and controlled study. The investigators will Randomize 728 patients with Chronic Kidney Disease(CKD) stage 3b (CKD-3b) and CKD stage 4: 364 of these patients will be included in the study group called Bicarbonate Group (Bic), in which levels of bicarbonate should be kept > 24 mEq/l; the other 364 patients will included in the Usual Treatment Group (no-Bic). Results: The aim of the Research Protocol is to demonstrate if that the optimal correction of uremic acidosis (with administration of sodium bicarbonate or of any other alkalinizing agent, e.g. sodium citrate) reduces renal and cardiovascular mortality. Conclusions. In conclusion the Work Group of the Conservative Therapy for Chronic Renal Insufficiency proposes this cohort, randomized, controlled, prospective, multicentric study to evaluate the effects of correction of acidosis on the progression of the kidney disease considered as renal death in End-Stage Renal Disease (ESRD) patients.

NCT ID: NCT01506258 Recruiting - Clinical trials for Multiple Organ Failure

Autologous Stem Cells in Newborns With Oxygen Deprivation

Start date: January 2012
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether the plasticity of autologous intravenous application of cord blood stem cells would improve the clinical course of asphyxiated newborns.

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.