Trajectories of Recovery After Intravenous Propofol Versus Inhaled VolatilE Anesthesia Trial

Description

The investigators will conduct a 12,500-patient randomized multi-center trial to determine (i) which general anesthesia technique yields superior patient recovery experiences in any of three surgical categories ((a) major inpatient surgery, (b) minor inpatient surgery, (c) outpatient surgery) and (ii) whether TIVA confers no more than a small (0.2 %) increased risk of intraoperative awareness than INVA in patients undergoing both outpatient and inpatient surgeries

Conditions

Surgery-Complications, Anesthesia Complication, Anesthesia Awareness, Anesthesia, Surgery, Quality of Life, Pain, Postoperative, Anesthesia Morbidity

Study Overview

Study Details

Study overview

The investigators will conduct a 12,500-patient randomized multi-center trial to determine (i) which general anesthesia technique yields superior patient recovery experiences in any of three surgical categories ((a) major inpatient surgery, (b) minor inpatient surgery, (c) outpatient surgery) and (ii) whether TIVA confers no more than a small (0.2 %) increased risk of intraoperative awareness than INVA in patients undergoing both outpatient and inpatient surgeries

Trajectories of Recovery After Intravenous Propofol Versus Inhaled VolatilE Anesthesia Trial

Trajectories of Recovery After Intravenous Propofol Versus Inhaled VolatilE Anesthesia Trial

Condition
Surgery-Complications
Intervention / Treatment

-

Contacts and Locations

Little Rock

University of Arkansas for Medical Sciences (UAMS), Little Rock, Arkansas, United States, 72205

San Francisco

University of California San Francisco, San Francisco, California, United States, 94143

Stanford

Stanford University, Stanford, California, United States, 94305

New Haven

Yale School of Medicine, New Haven, Connecticut, United States, 06510

Boston

Massachusetts General Hospital, Boston, Massachusetts, United States, 02114

Boston

Brigham & Women's, Boston, Massachusetts, United States, 02115

Ann Arbor

University of Michigan, Ann Arbor, Michigan, United States, 48109

Detroit

Henry Ford Health, Detroit, Michigan, United States, 48202

Saint Louis

Washington University School of Medicine, Saint Louis, Missouri, United States, 63110

Lebanon

Dartmouth Hitchcock Medical Center, Lebanon, New Hampshire, United States, 03756

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

    Ages Eligible for Study

    18 Years to

    Sexes Eligible for Study

    ALL

    Accepts Healthy Volunteers

    No

    Collaborators and Investigators

    Washington University School of Medicine,

    Sachin Kheterpal, MD, PRINCIPAL_INVESTIGATOR, University of Michigan

    Michael S Avidan, MBBCh, PRINCIPAL_INVESTIGATOR, Washington University School of Medicine

    Allison Janda, MD, STUDY_DIRECTOR, University of Michigan

    Mark Neuman, MD, STUDY_DIRECTOR, University of Pennsylvania

    Bethany Pennington, PharmD, STUDY_DIRECTOR, Washington University School of Medicine

    Douglas Colquhoun, MBChB, STUDY_DIRECTOR, University of Michigan

    Study Record Dates

    2028-07-31