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TerminatedNo phase

The Effect of Continued Mechanical Ventilation on the Occurrence of Myocardial Ischemia

Key facts

Who runs it
Jessa Hospital
Where
Belgium1 site in 1 countryChoose a country to see its sites
Trial code
Status
Terminated
People taking part
165 people enrolled
Started
17 Oct 2022
Ended
9 Nov 2024
Type of study
Interventional, 2 groupsOne group gets an existing treatment, for comparison.
Treatments tested
  • Discontinued ventilation
  • Continued ventilation
Record updated
29 November 2024
Why it stopped
After the passing of the principal investigator, the clinical trial could not be continued.

Who can take part

Age
18 years and older
Sex
Women and men
Healthy volunteers
Cannot take part

The registry criteria, word for word

Show all 9 criteriaShow less

Who can take part

  • Patients older than 18 years old
  • Patients undergoing their first elective endo-CABG procedure using peripheral cannulation for CPB
  • Patients who are able to give their informed consent
  • Patients who speak Dutch or French

Who cannot take part

  • Patients taking corticosteroids
  • Patients with lung diseases (chronic obstructive pulmonary disease (COPD), asthma)
  • Patients with an ejection fraction < 25%
  • Patients participating in another clinical trial
  • Patients where groin cannulation is not possible

This trial has no sites in United States.

It has sites in one country. Choose a country to see its sites.

About the trial

What the trial wants to find out

The goal of this study is to examine the influence of mechanical ventilation on the occurrence of myocardial ischemia in patients undergoing endo-CABG.

The 2 groups in the trial

  • Control groupExisting treatment, for comparison

    Ventilation is discontinued after going on CPB and lungs are exposed to atmospheric pressure. Blood will be drawn: At baseline: before general anaesthesia, after start of CPB, after clamping the aorta, before unclamping the aorta, after the operation, 5 h after clamping the aorta, 12 hours after clamping the aorta, and 24 hours after aortic clamping

    Treatment: Discontinued ventilation

  • Ventilation groupTreatment being tested

    Ventilation is continued from going on CPB until clamping of the ascending aorta. Blood will be drawn: At baseline: before general anaesthesia, after start of CPB, after clamping the aorta, before unclamping the aorta, after the operation, 5 h after clamping the aorta, 12 hours after clamping the aorta, and 24 hours after aortic clamping

    Treatment: Continued ventilation

Data and sources

Registry record
Listed on ClinicalTrials.gov.
Official title
The Effect of Continued Mechanical Ventilation on the Occurrence of Myocardial Ischemia in Patients Undergoing Totally Endoscopic Coronary Artery Bypass Grafting
Record updated
29 November 2024