Study Overview
This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.
Description
The investigators will conduct a 13,000-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
Official Title
Trajectories of Recovery After Intravenous Propofol Versus Inhaled VolatilE Anesthesia Trial
Quick Facts
Study Start:2023-09-13
Study Completion:2028-07-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING
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.
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Contacts and Locations
Study Locations (Sites)
University of Arkansas for Medical Sciences (UAMS)
Little Rock, Arkansas, 72205
United States
University of California San Francisco
San Francisco, California, 94143
United States
Stanford University
Stanford, California, 94305
United States
Yale School of Medicine
New Haven, Connecticut, 06510
United States
Massachusetts General Hospital
Boston, Massachusetts, 02114
United States
Brigham & Women's
Boston, Massachusetts, 02115
United States
University of Michigan
Ann Arbor, Michigan, 48109
United States
Henry Ford Health
Detroit, Michigan, 48202
United States
Washington University School of Medicine
St. Louis, Missouri, 63110
United States
Dartmouth Hitchcock Medical Center
Lebanon, New Hampshire, 03756
United States
NYU Langone
New York, New York, 10012
United States
Weill Cornell Medicine
New York, New York, 10065
United States
Duke University
Durham, North Carolina, 27708
United States
Wake Forest
Winston-Salem, North Carolina, 27109
United States
Oregon Health and Sciences University
Portland, Oregon, 97239
United States
University of Pennsylvania
Philadelphia, Pennsylvania, 19104
United States
University of Texas - MD Anderson
Houston, Texas, 77030
United States
University of Utah - Medical
Salt Lake City, Utah, 84132
United States
UVA Health
Charlottesville, Virginia, 22908
United States
University of Washington
Seattle, Washington, 98195
United States
Collaborators and Investigators
Sponsor: 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
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Registration Dates
Study Start Date2023-09-13
Study Completion Date2028-07-31
Study Record Updates
Study Start Date2023-09-13
Study Completion Date2028-07-31
Terms related to this study
Additional Relevant MeSH Terms
- Surgery-Complications
- Anesthesia Complication
- Anesthesia Awareness
- Anesthesia
- Surgery
- Quality of Life
- Pain, Postoperative
- Anesthesia Morbidity