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Lactate Metabolism in the Hypoperfused Critically Ill

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University of Copenhagen

Status

Enrolling

Conditions

Metabolism
Metabolomics
Hypoperfusion
Lactate
Metabolic Acidosis

Treatments

Other: Blood and urine test

Study type

Observational

Funder types

Other

Identifiers

NCT05582824
LacMeta

Details and patient eligibility

About

Investigating lactate metabolism in critically ill patients whom are hypoperfused by preforming metabolomics via liquid chromatography-mass spectrometry.

Full description

Lactate concentration is well known to be directly correlated with risk of death during admission to intensive care. However, lactate by itself is not considered toxic. The study is observational. The breakdown of lactate is being investigated by collecting blood- and urinsamples from patients with hyperlactatemia as a result of hypoperfusion. Levels of lactate, and known as well as unknown metabolites will be identified and quantified by metabolomics. Metabolomics is performed using a combination of liquid chromatography and mass spectrometry. Data will be analysed via statistical analysis to investigate corelations between lactate, a given metabolite and hard outcome such as mortality. And thereby lay the groundwork for potential further research regarding specific lactate-metabolites.

Enrollment

20 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Diagnosed with sepsis/septic shock or severe heart failure.
  • Clinical and paraclinical signs of hypoperfusion in relation to abovementioned diagnosis.
  • Metabolic acidosis with s-lactate equal-to-or-above 4 mmol/l.
  • Incapacitated

Exclusion criteria

  • Only regional hypoperfusion such as a leg.
  • Receiving intravenous lactate as part of treatment.
  • Going in to dialysis. The exclusion is only during dialysis treatment.

Trial design

20 participants in 1 patient group

Main group
Description:
All patients included
Treatment:
Other: Blood and urine test

Trial contacts and locations

1

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Central trial contact

Henrik Wolsted, MD; Jesper H Kilbak, Stud. scient.

Data sourced from clinicaltrials.gov

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