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Hypotension Prediction Index in Postoperative Surgical Patients (HPI-PACU)

S

Sir Mortimer B. Davis - Jewish General Hospital

Status

Enrolling

Conditions

Surgery

Treatments

Device: Device: HemoSphere monitor and Acumen IQ sensor.

Study type

Observational

Funder types

Other

Identifiers

NCT05335174
2022-3143

Details and patient eligibility

About

PACU-HPI study evaluates the use of a hemodynamic monitor in the post-anesthetic recovery room on patients undergoing colorectal, hepatobiliary, and vascular surgery, to determine the feasibility of recruiting this surgical population.

Full description

Postoperative vascular complications, including myocardial infarction (MI), myocardial injury after noncardiac surgery (MINS), stroke, and death occur in up to 18% of surgical patients.1 Hypotension is a frequent occurrence in the postoperative period and can increase the risk of postoperative vascular complications.2 Therefore, accurate prediction of postoperative hypotension can identify patients at risk for postoperative vascular complications who would benefit from early intervention. The investigators propose a feasibility study to determine the accuracy of the hypotension prediction index (HPI) parameter of the HemoSphere monitor and Acumen IQ sensor (Edwards Lifesciences, Irvine, CA) to predict postoperative hypotension in surgical patients.

Enrollment

30 estimated patients

Sex

All

Ages

45+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Patient ≥45 years old
  2. Will undergo open colorectal, hepatobiliary, or vascular surgery;
  3. Is expected to have an arterial cannula inserted intraoperatively;
  4. Has an anticipated stay in PACU for at least 2 hours;
  5. Able to provide written informed consent

Exclusion criteria

  1. Planned admission to ICU;
  2. Refusal to participate;
  3. Previously enrolled in the study

Trial design

30 participants in 1 patient group

HPI monitor
Treatment:
Device: Device: HemoSphere monitor and Acumen IQ sensor.

Trial contacts and locations

1

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Central trial contact

Mirana Rakotoarivony; Stephen Yang, MD, MSc

Data sourced from clinicaltrials.gov

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