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Completed

NCT Number: NCT01981655

0.5M Na Lactate Solution in Acute Heart Failure (AHF)

The objective of this trial to see whether:

-Cardiac performance (cardiac index and secondary outcomes)can be improved in patients with acute heart failure (AHF) and symptoms and consequences of fluid overload (pulmonary and interstitial edema) and poor peripheral perfusion can be reduced by:

1. Providing lactate as a substrate(Improve cardiac index) 2. Simultaneously restoring optimal preload

Optimal standard treatment will be achieved in both arms with the use of current best treatment protocol for AHF as per independent treating physician.

4. To assess effects of 0.5M Na lactate (Totilac) on plasma and urine biological parameters (sodium, potassium, chloride, pH, bicarb, base excess, albumin)

5. To assess effects of 0.5M Na lactate on morbidity and mortality.

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Key information

Conditions

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Dept. of Intensive Care, Nepean Hosp., U Sydney

Penrith, New South Wales, 2751, Australia

About this study

  • Acute heart failure is a critical illness for which current treatments are suboptimal.
  • The various symptoms are related to inadequate cardiac output and usually include left ventricular overload with pulmonary oedema, interstitial fluid accumulation and tissue oedema (as indicated by frequent hyponatremia and hypoalbuminemia) and insufficient peripheral perfusion frequently manifesting as cold extremities and low urine output.
  • The current treatment of this syndrome is based on diuretics, vasodilators and/or inotropes, but fluid administration is also required to optimise the intravascular volume state and to reverse shock if present. Therefore management of body fluid balance remains a challenge since treatment aims to simultaneously maintain or improve intravascular volume and decrease body fluid excess and oedema.
  • The purpose of the present study is to assess in a prospective randomised trial the efficacy and safety of a newly designed crystalloid solution, 0.5 M sodium lactate, with properties potentially able to improve multiple pathophysiological aspects of AHF, as compared to the use of standard crystalloid solution Compound Sodium Lactate (mildly hypoosmolar ~ 274 mOsm/L and isotonic).

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age: more than 18 years
  • Heart failure criteria:

Left heart failure: as evidenced by 2 out of 3:

  • Left ventricular ejection fraction (LVEF) ≤ 40% and cardiac index ≤ 2.5 L/min/m2
  • Acute pulmonary oedema of cardiac origin or mechanical ventilation (including CPAP/BIPAP) for respiratory failure of predominantly cardiac origin
  • Need for inotropes/vasopressors for cardiac pump failure OR

Right heart failure: as evidenced by 1 out of 2:

  • Bilateral leg oedema above ankles
  • RV failure (low tricuspid annular plane systolic excursion (TAPSE), dilated floppy RV)
  • Poor peripheral perfusion as evidenced by 2 out of 3:

Cold mottled skin Low urine output Acutely clouded sensorium/poor mentation

  • Consent obtained from patient or patient's next of kin.

Exclusion criteria

  • Hypernatremia: [Na] >145 mmol/L
  • Diagnosed hypertrophic obstructive cardiomyopathy
  • Uncorrected severe valvular heart disease
  • Documented third degree heart block, sustained ventricular tachycardia
  • Documented cardiac tamponade
  • Septic shock
  • Acute respiratory distress syndrome (ARDS)
  • Moribund patients likely to die before 24h
  • Patients with major diseases of limited prognosis such as end stage cancer,end-stage liver failure, end stage dialysis dependent renal failure
  • Patients with absolute indication for acute hemodialysis/hemofiltration (pH, K, urea > 35 mmol/L, severe fluid overload in the presence of oliguria < 200 mL/6h.
  • Known pregnancy

Treatment and study plan

0.5M Sodium lactate

Drug

A bolus of 0.5M Sodium lactate of 3 ml per kg BW is administered in 15 minutes, followed by a continuous infusion with 1 ml per kg per hour for 24 hours, i.e. in total 27 ml per kg over 24 hours

Other names: Totilac

Hartmann's solution

Drug

Hartmann's solution of 3 ml per kg BW is administered in 15 minutes, No infusion thereafter i.e. in total 3 ml per kg over 24 hours

Other names: Compound Sodium Lactate

Primary outcomes

  1. Efficacy

    Time frame: Baseline till 24 hours from first loading of study drug

    Improvement in cardiac output measured by transthoracic echocardiography at 24 hours from initiation of study drug infusion

Secondary outcomes

  1. mortality

    Time frame: up to 3 month

    range of efficacy and safety parameters

  2. acid base and electrolytes, fluid balance

    Time frame: 48 hours

    the effect on on pH, base excess, bicarbonate, sodium, potassium, phosphate, chloride and lactate will be assessed during the study period

  3. organ function

    Time frame: 48 hours

    effect on respiratory function assessed by time on ventilatory support and renal function measured by creatinine level over 48 hours will be assessed

Sponsors and collaborators

Lead sponsor

Nepean Blue Mountains Local Health District

Other

Collaborators

  • Innogene Kalbiotech Pte. Ltd

Registry information

Official study title

A Phase 2, Randomised, Single-Blind, Placebo-controlled Study of Half Molar Sodium Lactate Solution in the Treatment of Subjects With Acute Heart Failure

Acronym: SOLACE1

Important dates

Study start
2009
Primary completion
2013
Study completion
2013
First posted
Nov 11, 2013
Registry last updated
Nov 13, 2013

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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