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Corticosteroid
Anesthesia Types for Cancer Surgery (GA-CARES Trial)
Phase 4
Waitlist Available
Research Sponsored by Stony Brook University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
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
Be older than 18 years old
Must not have
Age less than 18 years
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 2 year minimum
Awards & highlights
Pivotal Trial
Drug Has Already Been Approved
No Placebo-Only Group
Summary
This trial is testing two ways to keep patients asleep during cancer surgery: one using an IV drug called propofol and the other using inhaled gases. It aims to see which method is better at reducing the risk of death from any cause. Propofol is a widely used intravenous anesthetic known for its potential effects on cancer outcomes.
Who is the study for?
The GA-CARES trial is for adult cancer patients undergoing specific surgeries like lung, esophagus, bladder, pancreas removal or certain chemo procedures. It's not for those under 18, with a very short life expectancy, severe health issues (ASA Class 5), egg/soy allergies, or sensitivity to anesthesia.
What is being tested?
This study compares two ways of keeping people asleep during cancer surgery: using propofol through an IV or inhaling agents like sevoflurane. The goal is to see which method affects survival rates after surgery.
What are the potential side effects?
Propofol may cause low blood pressure, pain at the injection site and can lead to a rare but serious condition called Propofol Infusion Syndrome. Inhaled agents might lower blood pressure and heart rate and could cause nausea or vomiting after waking up.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I am scheduled for a major cancer surgery, such as lung, esophagus, bladder, pancreas, liver, stomach removal or specific chemotherapy.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I am under 18 years old.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 2 year minimum
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~2 year minimum
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
All-cause mortality
Secondary study objectives
Recurrence free survival
Awards & Highlights
Pivotal Trial
The final step before approval, pivotal trials feature drugs that have already shown basic safety & efficacy.
Drug Has Already Been Approved
The FDA has already approved this drug, and is just seeking more data.
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
2Treatment groups
Experimental Treatment
Group I: Volatile agentExperimental Treatment1 Intervention
Maintenance of general anesthesia with volatile agent (sevoflurane, desflurane, or isoflurane)
Group II: Propofol infusionExperimental Treatment1 Intervention
Maintenance of general anesthesia with propofol infusion
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Propofol
2017
Completed Phase 4
~1520
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
The most common treatments for general anesthesia include Total Intravenous Anesthesia (TIVA) using Propofol and Volatile Agents such as sevoflurane, isoflurane, and desflurane. Propofol works by enhancing the activity of gamma-aminobutyric acid (GABA) receptors, the major inhibitory neurotransmitters in the brain, leading to sedation and hypnosis.
Volatile agents induce central nervous system depression by enhancing GABA activity and affecting other ion channels, which decreases neuronal excitability. Understanding these mechanisms is crucial for tailoring anesthesia plans to individual patient needs, optimizing safety, and improving recovery outcomes.
Sevoflurane and propofol increase 11C-flumazenil binding to gamma-aminobutyric acidA receptors in humans.
Sevoflurane and propofol increase 11C-flumazenil binding to gamma-aminobutyric acidA receptors in humans.
Find a Location
Who is running the clinical trial?
Stony Brook UniversityLead Sponsor
222 Previous Clinical Trials
40,227 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I am scheduled for a major cancer surgery, such as lung, esophagus, bladder, pancreas, liver, stomach removal or specific chemotherapy.I am under 18 years old.
Research Study Groups:
This trial has the following groups:- Group 1: Volatile agent
- Group 2: Propofol infusion
Awards:
This trial has 3 awards, including:- Pivotal Trial - The final step before approval, pivotal trials feature drugs that have already shown basic safety & efficacy.
- Drug Has Already Been Approved - The FDA has already approved this drug, and is just seeking more data.
- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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