Dept. of Intensive Care, Nepean Hosp., U Sydney
Penrith, New South Wales, 2751, Australia
NCT Number: NCT01981655
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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Notify Me18 year and older
All sexes
Interventional
Phase 2
Penrith, New South Wales, 2751, Australia
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Left heart failure: as evidenced by 2 out of 3:
Right heart failure: as evidenced by 1 out of 2:
Cold mottled skin Low urine output Acutely clouded sensorium/poor mentation
Exclusion criteria
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 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
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
Time frame: up to 3 month
range of efficacy and safety parameters
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
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
Nepean Blue Mountains Local Health District
Other
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
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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