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Postoperative DeliriumNCT03117712

Cerebral Blood Supply During Cardiopulmonary Bypass

An observational study of Postoperative Delirium, run by Medical University of Vienna at 1 site in Austria.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

Postoperative delirium is an acute and fluctuating state of confusion and disorientation with an incidence of 25-70% after cardiac surgery. Possible reasons for this multifactorial complication are hypoperfusion, cerebral microembolization and inflammatory response, which eventually lead to regional or global… Read more about this study

Who is it for?
Ages 18 to 100 years
Conditions the study is for
Postoperative Delirium
What is being tested?
Delirium Scores, Carotis duplex sonography and TCD for detection of HITS
How many people
40 participants
Where
1 siteAustria
Study dates
1 May 2017to 31 Dec 2018
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 100 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: Elective cardiac surgical patients undergoing valve replacement/reconstruction surgery on cardiopulmonary bypass.

Who may be able to join

  • elective cardiac surgery valve replacement/reconstruction cardiopulmonary bypass

Who cannot join

  • Emergency procedures
  • Postoperative need for extracorporal cardiac assist device
  • Untreated or uncontrolled arterial hypertension
  • Profound hypothermic CPB (body temperature <34°C)
  • History of preoperative dementia
  • History of Stroke
Show all 10Show fewer
  • Significant carotid artery stenosis
  • Age < 18 years
  • Chronic renal replacement therapy
  • Declined informed consent

Trial locations and contacts

1 site in 1 country.

Austria1 site
  • Medical university of vienna, General hospital of Vienna

    Vienna, 1090

Other trials in Austria

About this study

Official title: Influence of Cerebral Blood Supply During Cardiopulmonary Bypass on the Incidence of Postoperative Delirium in Open-heart Surgery

Postoperative delirium is an acute and fluctuating state of confusion and disorientation with an incidence of 25-70% after cardiac surgery. Possible reasons for this multifactorial complication are hypoperfusion, cerebral microembolization and inflammatory response, which eventually lead to regional or global imbalance between cerebral oxygen demand and supply. Adequate cerebral blood supply depends sufficient blood supply via the vertebral arteries and the internal carotid arteries. The aim of this preliminary study is to investigate if patients who develop delirium after open-heart surgery show differences in their cerebral blood flow during cardiopulmonary bypass (CPB) in extracerebral arterial vessels compared to those patients without delirium.

Read the detailed description

Postoperative delirium is an acute and fluctuating state of confusion and disorientation, characterized by changes in attention, cognition, consciousness, and perception, with an incidence of 25-70% after cardiac surgery. Possible reasons for this multifactorial complication are hypoperfusion, cerebral microembolization and inflammatory response, which eventually lead to regional or global imbalance between cerebral oxygen demand and supply. This frequent cerebral injury has detrimental and long-lasting consequences and remains a serious healthcare burden, particularly due to its association with higher medical costs, increased morbidity, long-term cognitive deficits, and greater mortality. Progress in reducing the incidence of delirium has been hindered by the lack of a full understanding of its pathophysiology.

Adequate cerebral blood supply depends sufficient blood supply via the vertebral arteries and the internal carotid arteries. Whereby the blood supply of the brain by the carotid arteries is two-thirds and is easily accessable for blood flow examination with Doppler ultrasound.

The aim of this preliminary study is to investigate if patients who develop delirium after open-heart surgery show differences in their cerebral blood flow during cardiopulmonary bypass (CPB) in extracerebral arterial vessels compared to those patients without delirium. Additionally we want to investigate the influence of cerebral microembolisation and CPB associated inflammation in those patients. As secondary outcome measure we also want to determine differences in length of stay (LOS) in the intensive care unit (ICU) as well as in hospital LOS and 30-day mortality.

Methods:

Design:

Prospective observational study

Population:

Elective cardiac surgical patients undergoing valve replacement/reconstruction surgery on cardiopulmonary bypass.

Procedure:

Patients will be enrolled the day before surgery by one physician of the study group.

Anaesthesia will be induced with propofol (1.0-1.5 mg/kg), fentanyl (3-10 μg/kg), and cisatracurium (0.2 mg/kg). It will be maintained with sevoflurane (target BIS value 40-50) 11, and fentanyl (0.05-0.1 μg/kg/min). Patients will receive tranexamic acid (10 mg/kg after anaesthesia induction plus the same dosage in the CPB prime), depending on their kidney function.

Anticoagulation will be achieved with heparin (400 IE/kg) to an activated clotting time (ACT) >400 s.

CPB will be performed using non-pulsatile target flow of 100% calculated cardiac output. Mean arterial pressure will be maintained between 60 to 70 mmHg throughout CPB.

To standardize the intraoperative course of our patients we will limit the intraoperative haematocrit to 22% and the PaCO2-concentration between 30 and 40 mmHg.12 Blood glucose levels will be held between 80-150 mg/dl intra- and postoperatively. Sedation on ICU will be performed using propofol until extubation

Carotis duplex sonography for perfusion flow will be evaluated at the following timepoints:

  1. Before induction of anaesthesia
  2. Before going on CBP
  3. During CPB, 5 min after aortic cross clamping
  4. After CPB
  5. 24 hours after CPB Blood flow will be derived from the product of the vessels' cross-sectional area and the intensity-weighted mean blood flow velocity through the vessel using a pulsed-wave Doppler in ml/min. Because the sample volume will be adjusted to the width of the vessel at the point where the diameter width will be measured, the measurement can be performed independent of flow conditions (laminary or pulsatile). Imaging of the vessel will be performed in the longitudinal plane, the cross-sectional area will be assumed to be circular.

To diagnose postoperative delirium two delirium assessement tests will be used:

  • Confusion Assessment method for the ICU (CAM-ICU) and
  • The Intensive Care Delirium Screening Checklist (ICDSC)

Delirium Scores will be measured at the following timepoints:

  1. Postoperative day (POD) 1
  2. POD 2
  3. POD 5

The CAM-ICU will be assessed twice a day (in the morning and in the evening). The Confusion Assessment Method (CAM) will be performed after discharge from the ICU.

Transcranial Doppler ultrasound (TCD) for detection and differentiation of high-intensity transient signals (HITS) in both middle cerebral arteries (MCAs) into artefacts, solid, and gaseous cerebral microemboli (CME) will be performed at the following timepoints:

  1. During cannulation of the ascending aorta
  2. After aortic cross-clamp
  3. During decannulation All collected data will be saved password-protected in an electronic database on the department's server after data collection has been finished. Only studyteam-members will have access to this data. After completion of the study the results are to be published according to GCP-standards.
Being tested
Delirium Scores, Carotis duplex sonography, TCD for detection of HITS
Keywords
cerebral blood supply, cardiopulmonary bypass, open-heart cardiac surgery
Medical subject headings
Emergence Delirium

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Delirium ScoresDiagnostic test

    • Confusion Assessment method for the ICU (CAM-ICU) and
    • The Intensive Care Delirium Screening Checklist (ICDSC)

    Delirium Scores will be measured at the following timepoints:

    1. Postoperative day (POD) 1
    2. POD 2
    3. POD 5
  • Carotis duplex sonographyDiagnostic test

    Carotis duplex sonography for perfusion flow will be evaluated at the following timepoints:

    1. Before induction of anaesthesia
    2. Before going on cardiopulmonary bypass (CBP)
    3. During CPB, 5 min after aortic cross clamping
    4. After CPB
    5. 24 hours after CPB
  • TCD for detection of HITSDiagnostic test

    Transcranial Doppler ultrasound (TCD) for detection and differentiation of high-intensity transient signals (HITS) in both middle cerebral arteries (MCAs) into artefacts, solid, and gaseous cerebral microemboli (CME) will be performed at the following timepoints:

    1. During cannulation of the ascending aorta
    2. After aortic cross-clamp
    3. After opening of the aortic cross-clamp
    4. During decannulation
Study groups in NCT03117712
Study groupRoleWhat they receive
Deliriumpatients who develop postoperative delirium after surgery with cardiopulmonary bypass measured by Delirium scores (CAM-ICU, ICDSC), TCD for detection of HITS and carotis duplex sonography
Receives: Diagnostic Test: Delirium Scores; Diagnostic Test: Carotis duplex sonography; Diagnostic Test: TCD for detection of HITS
No deliriumpatients who develop no postoperative delirium after surgery with cardiopulmonary bypass measured by delirium scores (CAM-ICU, ICDSC), TCD for detection of HITS and carotis duplex sonography
Receives: Diagnostic Test: Delirium Scores; Diagnostic Test: Carotis duplex sonography; Diagnostic Test: TCD for detection of HITS

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. cerebral blood flow

    Differences in mean laminar cerebral blood flow on cardiopulmonary bypass during open heart surgery between patients with and without postoperative delirium

    Measured: during surgery

Secondary outcomes (1)
  1. HITS (high-intensity transient signals)

    Difference in the number and quality of HITS measured with transcranial Doppler ultrasound between patients with and without delirium

    Measured: during surgery

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted18 Apr 2017
  2. Study start1 May 2017
  3. Primary completion30 Jun 2018
  4. Study completion31 Dec 2018

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
40 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT03117712
Sponsor's protocol ID
1964/2016
Status last verified
Mar 2019
First submitted
6 Apr 2017
Last updated
6 Mar 2019
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

An observational study of Postoperative Delirium, run by Medical University of Vienna at 1 site in Austria.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 10 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 6 Mar 2019. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Austria. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

cerebral blood flow (time frame: during surgery). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 6 Mar 2019; AzTrials last refreshed its copy on 6 Nov 2026.

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