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临床试验/NCT04934683
NCT04934683Enrolling By Invitation4 期

Tight Perioperative Blood Pressure Management to Reduce Serious Cardiovascular, Renal, and Cognitive Complications: The GUARDIAN Trial (Induction Agent Sub-Study Comparing Etomidate and Propofol)

The University of Texas Health Science Center, Houston11 个研究点 分布在 4 个国家目标入组 6,254 人开始时间: 2021年7月25日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
Enrolling By Invitation
入组人数
6,254
试验地点
11
主要终点
Number of Participants with a Composite of Major Perfusion-Related Complications

研究概览

简要总结

This is a sub-study of the overall GUARDIAN trial (NCT04884802) in which some GUARDIAN trial participants will be additionally randomized to etomidate vs propofol for anesthetic induction.

详细描述

Participants in the underlying GUARDIAN trial (NCT04884802) will be randomized to: 1) routine intraoperative blood pressure management (routine pressure management); or 2) norepinephrine or phenylephrine infusion to maintain intraoperative MAP ≥85 mmHg (tight pressure management). Participants in this sub-study will be additionally randomized to etomidate or propofol for induction of anesthesia.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Factorial
主要目的
Prevention
盲法
Double (Participant, Outcomes Assessor)

入排标准

年龄范围
45 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • At least 45 years old;
  • Scheduled for major noncardiac surgery expected to last at least 2 hours;
  • Having general anesthesia, neuraxial anesthesia, or the combination;
  • Expected to require at least overnight hospitalization (planned ICU admission is acceptable);
  • Are designated ASA physical status 2-4 (ranging from mild systemic disease through severe systemic disease that is a constant threat to life);
  • Expected to have direct intraoperative blood pressure monitoring with an arterial catheter;
  • Cared for by clinicians willing to follow the GUARDIAN protocol;
  • Subject to at least one of the following risk factors:
  • Age >65 years;
  • History of peripheral arterial disease;
  • History of coronary artery disease;
  • History of stroke or transient ischemic attack;
  • Serum creatinine >175 μmol/L (>2.0 mg/dl) within 6 months;
  • Diabetes requiring medication;
  • Current smoking or 15 pack-year history of smoking tobacco;
  • Scheduled for major vascular surgery;
  • Body mass index ≥35 kg/m2;
  • Preoperative high-sensitivity troponin T >14 ng/L or troponin I equivalent, defined as ≥15 ng/L (Abbott assay), 19 ng/L (Siemens assay, [Borges, unpublished]), or 25% of the 99% percentile for other assays - all within 6 months;
  • B-type natriuretic protein (BNP) >80 ng/L or N-terminal B-type natriuretic protein (NTProBNP) >200 ng/L within six months.

排除标准

  • Are scheduled for carotid artery surgery;
  • Are scheduled for intracranial surgery;
  • Are scheduled for partial or complete nephrectomy;
  • Are scheduled for pheochromocytoma surgery;
  • Are scheduled for liver or kidney transplantation;
  • Require preoperative intravenous vasoactive medications;
  • Have a condition that precludes routine or tight blood pressure management such as surgeon request for relative hypotension;
  • Require beach-chair positioning;
  • Have a documented history of dementia;
  • Have language, vision, or hearing impairments that may compromise cognitive assessments;
  • Have contraindications to norepinephrine or phenylephrine per clinician judgement;
  • Have previously participated in the GUARDIAN trial.

研究组 & 干预措施

Routine Blood Pressure Management and Propofol Induction

Active Comparator

Propofol will be used as the anesthetic induction agent.

干预措施: Propofol Induction (Drug)

Routine Blood Pressure Management and Propofol Induction

Active Comparator

Propofol will be used as the anesthetic induction agent.

干预措施: Routine Blood Pressure Management (Procedure)

Routine Blood Pressure Management and Etomidate Induction

Active Comparator

Etomidate will be used as the anesthetic induction agent.

干预措施: Routine Blood Pressure Management (Procedure)

Routine Blood Pressure Management and Etomidate Induction

Active Comparator

Etomidate will be used as the anesthetic induction agent.

干预措施: Etomidate Induction (Drug)

Tight Blood Pressure Management and Etomidate Induction

Active Comparator

Etomidate will be used as the anesthetic induction agent.

干预措施: Tight Blood Pressure Management (Procedure)

Tight Blood Pressure Management and Etomidate Induction

Active Comparator

Etomidate will be used as the anesthetic induction agent.

干预措施: Etomidate Induction (Drug)

Tight Blood Pressure Management and Propofol Induction

Active Comparator

Propofol will be used as the anesthetic induction agent.

干预措施: Tight Blood Pressure Management (Procedure)

Tight Blood Pressure Management and Propofol Induction

Active Comparator

Propofol will be used as the anesthetic induction agent.

干预措施: Propofol Induction (Drug)

结局指标

主要结局

Number of Participants with a Composite of Major Perfusion-Related Complications

时间窗: During the initial 30 days after major non-cardiac surgery

The primary outcome is a composite of major perfusion-related complications (myocardial injury, stroke, non-fatal cardiac arrest, Stage 2-3 acute kidney injury, deep or organ-space infection, sepsis, and death) in the 30 days after major non-cardiac surgery.

次要结局

  • Number of Participants with Postoperative Delirium(During the initial 4 postoperative days)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Daniel Sessler

Professor

The University of Texas Health Science Center, Houston

研究点 (11)

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