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Clinical Trials/NCT06225453
NCT06225453
Recruiting
Not Applicable

Effect of Individualized Versus Conventional Blood Pressure Management on Major Adverse Cardiac, Cerebrovascular, and Renal Events After Major Non-cardiac Surgery: Multicenter, Randomized Controlled Trial

Seoul National University Hospital5 sites in 1 country1,896 target enrollmentJanuary 29, 2024

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Major Non-cardiac Surgery
Sponsor
Seoul National University Hospital
Enrollment
1896
Locations
5
Primary Endpoint
The incidence of postoperative major adverse cardiac, cerebrovascular, and renal event
Status
Recruiting
Last Updated
11 months ago

Overview

Brief Summary

Study objective: To compare the effect of different perioperative blood pressure management strategies on major postoperative adverse outcomes / Study design: a multicenter, randomized controlled trial / Participants: 1896 patients undergoing major non-cardiac surgery / Methods: Patients are randomized into two groups, the individualized strategy (maintaining perioperative mean arterial pressure and systolic blood pressure more than -20% of their baseline values) or the conventional strategy (maintaining perioperative mean arterial pressure ≥65 mmHg and systolic blood pressure ≥90 mmHg in all patients). Then, the frequency of major postoperative adverse outcomes occurring within 7 postoperative days or before discharge (whichever occurs first). / Primary outcome: a composite of all-cause death, stroke, myocardial infarction, new or worsening congestive heart failure, unplanned coronary revascularization, and acute kidney injury, occuring within 7 postoperative days or before discharge (whichever occurs first).

Detailed Description

This study, aiming to reflect real clinical scenarios as much as possible, does not impose specific restrictions on perioperative management other than the target blood pressure. It allows discretion to each participating institution or physician. For the same reason, there are no restrictions on method for blood pressure measurement (invasive, non-invasive, or both), site of blood pressure measurement, fluid therapy, and vasopressors use for maintaining target blood pressure in each group. Through random allocation, the conventional group targets a mean arterial pressure (MAP) of 65 mmHg or higher and a systolic blood pressure (SBP) of 90 mmHg or higher during surgery. The individualized group targets no less than a -20% of the baseline MAP and SBP. The baseline MAP and SBP are defined as the average values of all MAP and SBP measured between one day before surgery and the morning of the surgery. The two blood pressure management strategies are applied until discharge from the post-anesthesia care unit. If the patient is transported to the intensive care unit after surgery, not the post-anesthesia care unit, then the blood pressure management strategies are applied until the end of surgery.

Registry
clinicaltrials.gov
Start Date
January 29, 2024
End Date
September 30, 2026
Last Updated
11 months ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Karam Nam, MD

Clinical Associate Professor

Seoul National University Hospital

Eligibility Criteria

Inclusion Criteria

  • Patients aged ≥65 or,
  • those aged ≥45 with a history of coronary artery disease, peripheral vascular disease, transient ischemic attack/stroke, or congestive heart failure,
  • undergoing non-cardiac surgery under general anesthesia with an anticipated duration of ≥2 hours.

Exclusion Criteria

  • Emergency surgery
  • Organ transplantation surgery
  • Brain/carotid artery surgery
  • American Society of Anesthesiologists physical status 5 or 6
  • Pregnancy
  • Uncontrolled preoperative hypertension (systolic blood pressure ≥180 mmHg or diastolic blood pressure ≥110 mmHg)
  • Estimated glomerular filtration rate \<30 ml/min/1.73m2
  • Renal replacement therapy
  • Acute decompensated heart failure
  • Use of inotropes/vasopressor infusion (dopamine, norepinephrine, vasopressin, etc.)

Outcomes

Primary Outcomes

The incidence of postoperative major adverse cardiac, cerebrovascular, and renal event

Time Frame: Occuring until discharge or postoperative day 7, whichever occurs first

A composite of all-cause death, stroke, myocardial infarction, new or worsening congestive heart failure, unplanned coronary revascularization, and acute kidney injury.

Secondary Outcomes

  • all-cause death(until discharge or postoperative day 7, whichever occurs first)
  • myocardial infarction(until discharge or postoperative day 7, whichever occurs first)
  • stroke(until discharge or postoperative day 7, whichever occurs first)
  • new or worsening congestive heart failure(until discharge or postoperative day 7, whichever occurs first)
  • acute kidney injury(until discharge or postoperative day 7, whichever occurs first)
  • Unplanned ICU admission(assessed from the end of surgery to hospital discharge (through study completion, generally of under one month))
  • new-onset atrial fibrillation(until discharge or postoperative day 7, whichever occurs first)
  • unplanned coronary revascularization(until discharge or postoperative day 7, whichever occurs first)
  • Length of postoperative hospital stay (days)(assessed from the end of surgery to hospital discharge (through study completion, generally of under one month))

Study Sites (5)

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