Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT05991453 · ClinicalTrials.gov registry record · NA
Trajectories of Recovery After Intravenous Propofol Versus Inhaled VolatilE Anesthesia Trial
A NA study of Surgery and Quality of Life, sponsored by Washington University School of Medicine.
- Recruiting
- Registry status
- NA
- Development phase
- 13,000
- Enrollment target
- 20
- Study locations
NCT05991453 is a NA study of Surgery and Quality of Life that is actively recruiting participants, run by Washington University School of Medicine. The registered enrollment target is 13,000 participants, below the 52,743-participant average among 120 other Surgery trials with a reported enrollment target (75% lower). The trial reports 20 study locations across 15 states.
The verdict
NCT05991453, a NA study of Surgery and Quality of Life, is actively recruiting participants, sponsored by Washington University School of Medicine.
- RECRUITING
- Registry status
- NA
- Development phase
- 13,000 participants
- Enrollment target
- 20
- Study locations
Study Summary
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
Conditions Studied
Interventions
- OTHER Anesthetic technique Propofol TIVA
- OTHER Anesthetic technique inhaled agent
Study Locations (20)
California
- University of California San Francisco - San Francisco
- Stanford University - Stanford
Massachusetts
- Massachusetts General Hospital - Boston
- Brigham & Women's - Boston
Michigan
- University of Michigan - Ann Arbor
- Henry Ford Health - Detroit
New York
- NYU Langone - New York
- Weill Cornell Medicine - New York
North Carolina
- Duke University - Durham
- Wake Forest - Winston-Salem
Arkansas
- University of Arkansas for Medical Sciences (UAMS) - Little Rock
Connecticut
- Yale School of Medicine - New Haven
Missouri
- Washington University School of Medicine - St Louis
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 13,000 participants |
| Start Date | 2023-09-13 |
| Est. Completion | 2028-07-31 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT05991453
The ClinicalTrials.gov registry entry for NCT05991453 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 13,000 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 52,743-participant average among 120 other Surgery trials with a reported enrollment target (75% lower). The listed sponsor is Washington University School of Medicine, which has 1,502 total studies on file at ClinicalTrials.gov.
The record links to 8 conditions, with Surgery appearing as the primary indexed condition, and to 2 interventions - of which Anesthetic technique Propofol TIVA is the first listed.
NCT05991453 reports 20 study locations spanning 15 distinct geographic areas - top geographies include California, Massachusetts, Michigan.
Frequently Asked Questions
What is clinical trial NCT05991453 about?
NCT05991453 is a clinical study titled "Trajectories of Recovery After Intravenous Propofol Versus Inhaled VolatilE Anesthesia Trial". 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 (i...
What is the current status of trial NCT05991453?
This trial is currently recruiting. It is a NA study. The enrollment target is 13,000 participants. The study started on 2023-09-13. Estimated completion is 2028-07-31.
What conditions does trial NCT05991453 study?
This clinical trial studies the following conditions: Surgery, Quality of Life, Pain, Postoperative, Anesthesia, Surgery--Complications.
What interventions are being tested in trial NCT05991453?
The interventions under investigation include: Anesthetic technique Propofol TIVA (OTHER), Anesthetic technique inhaled agent (OTHER).
Who is sponsoring clinical trial NCT05991453?
This trial is sponsored by Washington University School of Medicine, which has 1,502 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT05991453 being conducted?
This trial has 20 study locations across Arkansas, California, Connecticut, Massachusetts, Michigan. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for Surgery
Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
-
A Study of the Use of 3D Technology to Guide Head and Neck Surgery
RECRUITING · NA
-
INCLUDE Program: A Perioperative Wellness Program Tailored for Black Surgical Patients
RECRUITING · NA
-
Ultrasound Evaluation for Improving Patient Selection in vNOTES
RECRUITING · NA
-
Gastric US in ICU Patient
RECRUITING · NA
-
Intervention to Improve Utilization of Extended Venous Thromboembolism Prophylaxis After Cancer Surgery
RECRUITING · NA
-
Physical Therapy After Endometriosis Excision
RECRUITING · NA
Read our methodology - how this data is sourced, computed, and verified.
Related
Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.