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General Anesthetics in CAncer REsection Surgery (GA-CARES) Trial

General Anesthetics in CAncer REsection Surgery (GA-CARES) Trial: Pragmatic Randomized Trial of Propofol vs Volatile Inhalational Anesthesia

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03034096
Acronym
GA-CARES
Enrollment
1826
Registered
2017-01-27
Start date
2017-01-31
Completion date
2024-09-30
Last updated
2025-05-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anesthesia, General, Surgical Oncology

Brief summary

This is a large pragmatic multicenter trial comparing maintenance of general anesthesia with total intravenous anesthesia using propofol versus volatile agent (sevoflurane, isoflurane, or desflurane) during cancer surgery. The primary endpoint is all-cause mortality.

Interventions

DRUGPropofol

Maintenance of general anesthesia with propofol infusion

Maintenance of general anesthesia with volatile agent (sevoflurane, desflurane, or isoflurane)

Sponsors

Stony Brook University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients with known or suspected cancer and scheduled to undergo any of the following oncologic surgical procedures: * Lobectomy or pneumonectomy * Esophagectomy * Radical (total) cystectomy * Pancreatectomy * Partial hepatectomy * Hyperthermic intraperitoneal chemotherapy (HIPEC) * Gastrectomy (subtotal or total) * Cholecystectomy or bile duct resection

Exclusion criteria

* Age less than 18 years * American Society of Anesthesiologist Class 5 * Projected life expectancy less than 30 days * Known or suspected hypersensitivity to either propofol, e.g. egg or soy allergy, or volatile general anesthetic agents * Known or suspected history of malignant hyperthermia

Design outcomes

Primary

MeasureTime frameDescription
All-cause mortality2 year minimumTime to event

Secondary

MeasureTime frameDescription
Recurrence free survivalMinimum 2 yearsTime to event
All-cause mortality as a binary outcome2 years

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 12, 2026