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Oxygen Consumption, Hypoperfusion and Organ Injury After Cardio-pulmonary Bypass (VO2-EPOC)

U

Uppsala University Hospital

Status

Enrolling

Conditions

Cardiac Surgery Requiring Cardiopulmonary Bypass

Treatments

Other: Oxygen consumption measurement

Study type

Observational

Funder types

Other

Identifiers

NCT06930443
284709 (Other Identifier)
FOU2025-00095

Details and patient eligibility

About

The goal of this observational study is to understand how oxygen consumption after heart surgery relates to blood flow problems and organ injury. The study focuses on patients over 18 years old who are having planned heart surgery with a heart-lung machine (cardiopulmonary bypass).

The main questions the study aims to answer are:

  1. How does oxygen consumption in the early hours after surgery relate to lactate levels (a sign of low oxygen supply to the tissues)?
  2. How is oxygen consumption linked to signs of poor blood flow and organ injury (such as heart, kidney, liver, brain, and gut damage)?

Researchers will measure oxygen consumption after surgery using a technique called indirect calorimetry. They will also track blood flow and oxygen use during surgery and check for signs of organ injury the day after the procedure. The study will include 65 participants. People with certain health conditions, like severe anemia, high lactate levels before surgery, or needing intensive care or extra oxygen supply before surgery, will not be included. By understanding how oxygen consumption relates to blood flow and organ injury, this research may help to better manage patients after heart surgery and reduce complications.

Enrollment

65 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Elective cardiac surgery requiring cardiopulmonary bypass

Exclusion criteria

  • Combined, redo or annuloplasty procedures
  • Surgical procedures involving other vascular cannulation than standard direct, such as bicaval or femoral cannulation
  • Preoperative hyperlactatemia (>2mmol/L) or anaemia (Hb <90 g/dL)
  • Preoperative need for supplementary oxygen or ICU care
  • Consent not obtainable.

Trial contacts and locations

1

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Central trial contact

Olle Lönnemark MD; Julia Jakobsson MD PhD

Data sourced from clinicaltrials.gov

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