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Completed

NCT Number: NCT05964374

Goal-Directed Therapy Following Cardiac Surgery

Pilot prospective randomized control trial comparing goal-directed therapy algorithm vs routine care in the intensive care unit following cardiac surgery.

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Key information

Conditions

Age range

18 year–99 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Foothills Medical Centre

Calgary, Alberta, T2N2T9, Canada

About this study

Rationale:

Goal-directed therapy (GDT) has been shown to reduce complications and length of stay on cardiac surgery patients. Unfortunately, the existing literature on GDT in CV surgery has several limitations, which creates uncertainty over the expected benefit of implementing this care element with high associated costs and impact on workflow. Hypotension Prediction Index (HPI) is a proprietary algorithm that utilizes pulse contour analysis from invasive arterial pressure monitoring to identify patients at risk for becoming hypotensive within 15 minutes. The algorithm was developed using machine learning on a large surgical/ICU data set, and then externally validated on non-cardiac and cardiac surgical patients. HPI, as part of a GDT algorithm, may allow healthcare providers to identify patients recovering from cardiac surgery who may benefit from optimization prior to becoming hypotensive and assist with selecting the most appropriate hemodynamic intervention.

Hypothesis:

Application of an HPI-based GDT algorithm will result in a difference in cumulative fluid administration over the first 24-hours of index ICU admission following cardiac surgery.

Study Design:

Unblinded randomized controlled trial pilot. Data will be used to inform/justify the feasibility, design, and implementation of a future multi-center randomized controlled trial.

Study Population:

Moderate or high-risk (EuroSCORE II > 2%), non-emergent, adult open-heart cardiac surgery patients. Heart transplant, durable VAD implantation, or patients who require post-operative MCS support will be excluded.

Sample size= 100 (50 control : 50 intervention)

Intervention:

Patients randomized to the intervention arm will be monitored using the HPI technology and be treated following a GDT algorithm when HPI is >50 for 48-hours or duration of invasive arterial monitoring (whichever occurs first). The GDT algorithm is a standardized approach to identifying abnormal hemodynamic parameters and administering a prescribed therapy in a step-wise fashion with fixed re-assessment intervals (see attached).

What will be different from routine care? :

  • Hemodynamic interventions (fluid, inotropic, or vasopressor therapy) will be administered when HPI > 50 rather than MAP < 65.
  • Choice of applied therapy (fluid, inotropic, or vasopressor therapy) will be guided by a GDT algorithm.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • ≥ 18 years of age
  • Planned cardiac surgery using cardiopulmonary bypass (sternotomy or MICS)
  • Preoperative European System for Cardiac Operative Risk Evaluation II (EuroSCORE II) of 2% or more.
  • Informed consent obtained.

Exclusion criteria

  • Emergency surgery
  • Patients who refuse participation
  • Patients who are unable to give informed consent
  • Patients who are having a heart or lung transplant.
  • Surgery for insertion of any ventricular assist device
  • Aortic arch procedures with any degree of debranching or hybrid with endovascular intervention in the ascending aorta +/- arch.
  • Patients who require MCS (including ECMO, Impella, or IABP) post-operatively
  • Patients on contact/droplet isolation.
  • Patients deemed excessively unstable and/or complex by their attending intensivist on arrival to the ICU.
  • If the post-operative arterial line MAP goal is not 65 mmHg.
  • Patients who suffer intra-operative mortality.

Treatment and study plan

Goal-directed therapy

Device

Goal-directed therapy using HemoSphere® monitor, Acumen® transducer, and Hypotension Prediction Index® algorithm (Edwards Lifesciences, Irvine, USA),

Primary outcomes

  1. 24-hour cumulative IV fluid administration

    Time frame: 24-hours

    Cumulative post-operative intravenous fluid administration over the first 24-hours of index ICU admission.

Secondary outcomes

  1. Fluid Administration

    Time frame: Duration of ICU stay, up to 30-days

    Daily average

  2. Fluid Administration

    Time frame: Duration of ICU stay, up to 30-days

    Cumulative

  3. Vasoactive medication administration

    Time frame: Duration of ICU stay, up to 30-days

    Daily average

  4. Vasoactive medication administration

    Time frame: Duration of ICU stay, up to 30-days

    Daily cumulative

  5. Vasoactive medication administration

    Time frame: Duration of ICU stay, up to 30-days

    Duration

  6. Hemodynamic parameters

    Time frame: 48-hours or when arterial line removed

    Incidence of HPI > 50 greater than 5-minutes

  7. Hemodynamic parameters

    Time frame: 48-hours or when arterial line removed

    Incidence of HPI > 85 greater than 5-minutes

  8. Hemodynamic parameters

    Time frame: 48-hours or when arterial line removed

    Incidence of MAP < 65 greater than 5-minutes

  9. Hemodynamic parameters

    Time frame: 24-hours

    Total Area Under the Curve (AUC) for HPI > 50

  10. Hemodynamic parameters

    Time frame: 48-hours or when arterial line removed

    Total Area Under the Curve (AUC) for HPI > 50

  11. Hemodynamic parameters

    Time frame: 24-hours

    Total Area Under the Curve (AUC) for HPI > 85

  12. Hemodynamic parameters

    Time frame: 48-hours or when arterial line removed

    Total Area Under the Curve (AUC) for HPI > 85

  13. Hemodynamic parameters

    Time frame: 24-hours

    Total Area Under the Curve (AUC) for MAP < 65

  14. Hemodynamic parameters

    Time frame: 48-hours or when arterial line removed

    Total Area Under the Curve (AUC) for MAP < 65

  15. Enrollment

    Time frame: 1-year

    Proportion of screened patients eligible for enrollment.

  16. Enrollment

    Time frame: 1-year

    Proportion of eligible patients who consent to participate.

  17. Study Protocol Compliance

    Time frame: 1-year

    Proportion of consented patients who complete all study assessments.

  18. Arterial Monitoring Reliability

    Time frame: 1-year

    Number of arterial catheters requiring replacement

  19. GDT algorithm compliance

    Time frame: 48-hours or when arterial line removed

    Time from HPI > 50 to application of an intervention

  20. GDT algorithm compliance

    Time frame: 48-hours or when arterial line removed

    Proportion of hemodynamic interventions applied for HPI > 50 that were recommended by the algorithm

  21. GDT algorithm compliance

    Time frame: 48-hours or when arterial line removed

    Proportion of hemodynamic interventions applied for MAP < 65 that would be recommended by the algorithm based on hemodynamic parameters.

  22. GDT algorithm compliance

    Time frame: 48-hours or when arterial line removed

    MD notifications prompted by the GDT algorithm and resulting actions

  23. GDT algorithm compliance

    Time frame: 48-hours or when arterial line removed

    Actions (therapies or investigations) prompted by an MD notification.

  24. GDT algorithm compliance

    Time frame: 48-hours or when arterial line removed

    Number of study protocol suspensions

  25. GDT algorithm compliance

    Time frame: 48-hours or when arterial line removed

    Duration of protocol suspensions

  26. GDT algorithm compliance

    Time frame: 48-hours or when arterial line removed

    Rationale for protocol suspensions

  27. End-organ dysfunction/injury

    Time frame: Index admission, up to 30-days

    Acute kidney injury

  28. End-organ dysfunction/injury

    Time frame: Index admission, up to 30-days

    Delirium

  29. End-organ dysfunction/injury

    Time frame: Index admission, up to 30-days

    Stroke

  30. End-organ dysfunction/injury

    Time frame: Index admission, up to 30-days

    Ileus

  31. End-organ dysfunction/injury

    Time frame: Index admission, up to 30-days

    Gut infarction

  32. End-organ dysfunction/injury

    Time frame: Index admission, up to 30-days

    Prolonged mechanical ventilation (> 24 hours)

  33. End-organ dysfunction/injury

    Time frame: Index admission, up to 30-days

    Deep sternal wound infection

  34. End-organ dysfunction/injury

    Time frame: Index admission, up to 30-days

    Any surgical site infection

  35. Transfusion

    Time frame: Index admission, up to 30-days

    Total red-blood cell administration

  36. Transfusion

    Time frame: Index admission, up to 30-days

    Total fresh-frozen plasma administration

  37. Transfusion

    Time frame: Index admission, up to 30-days

    Total platelet administration

  38. Transfusion

    Time frame: Index admission, up to 30-days

    Total albumin administration

  39. Mobilzation

    Time frame: Index admission, up to 30-days

    Time to first mobilization (dangle)

  40. Mobilzation

    Time frame: Index admission, up to 30-days

    Time to first mobilization (stand)

  41. Mobilization

    Time frame: Index admission, up to 30-days

    Time to first mobilization (walk)

  42. Hydration

    Time frame: Index admission, up to 30-days

    Time to first PO hydration

  43. Nutrition

    Time frame: Index admission, up to 30-days

    Time to first PO nutrition

  44. Patient-centered Outcome

    Time frame: Index admission, up to 10-days

    Quality of Recovery-15 (QOR-15) at post-op days 3, 5, 7, and 10.

  45. Patient-centered Outcome

    Time frame: Up to 1-year post-operative

    World Health Organization Disability Assessment Schedule (WHODAS 2.0) at baseline, 2-weeks, 30-days, 90-days, and 1-year.

  46. Patient-centered Outcome

    Time frame: Up to 1-year post-operative

    MacNew Questionnaire at baseline, 2-weeks, 30-days, 90-days, and 1-year.

  47. Patient-centered Outcome

    Time frame: Up to 1-year post-operative

    The Depression, Anxiety and Stress Scale - 21 Items (DASS-21) at baseline, 2-weeks, 30-days, 90-days, and 1-year.

  48. Patient-centered Outcome

    Time frame: 30-days

    Canadian Patient Experiences Survey on Inpatient Care (CPES-IC) at 30-days

  49. Length of Stay

    Time frame: Up to 1-year post-operative

    ICU length of stay

  50. Length of Stay

    Time frame: Up to 1-year post-operative

    Hospital length of stay

  51. Re-admission

    Time frame: 30-days

    Incidence of hospital re-admission within 30-days of index surgery

  52. Mortality

    Time frame: Up to 1-year post-operative

    7-day, 30-day, and 1-year mortality.

Sponsors and collaborators

Lead sponsor

University of Calgary

Other

Collaborators

  • University of Alberta

Registry information

Official study title

Goal-Directed Therapy (GDT) Using Hypotension Prediction Index (HPI) Following Cardiac Surgery: a Pilot Randomized Control Trial

Important dates

Study start
2023
Primary completion
2024
Study completion
2025
First posted
Jul 27, 2023
Registry last updated
May 14, 2026

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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