Actively Recruiting
Propofol and Etomidate Admixtures Comparisons Trial (PEAC Trial)
Led by University of Texas Southwestern Medical Center · Updated on 2026-01-20
200
Participants Needed
1
Research Sites
232 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The purpose of this study is to evaluate the hemodynamics and adverse event profile in comparison between two treatment arms, one using an admixture of propofol and etomidate at a ratio by volume of 25%/75% (P2E7), and one using an admixture of propofol and etomidate at a ratio by volume of 75%/25% (P7E2), for anesthesia during endoscopic procedures at the Clements University Hospital (CUH) endoscopy lab (Endo).
CONDITIONS
Official Title
Propofol and Etomidate Admixtures Comparisons Trial (PEAC Trial)
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adult patients aged 18 years or older
- Scheduled for an endoscopic procedure at Clements University Hospital with anesthesia
- American Society of Anesthesiologists (ASA) classification of 3 or above
- Ejection fraction test result available
You will not qualify if you...
- Known allergies or adverse reactions to propofol, etomidate, their components, or preservatives
- Patient refusal to participate
- Clinician refusal to enroll the patient
- Documented cognitive impairments that prevent the patient from consenting, unless a legal surrogate consents
- Prisoners, incarcerated individuals, or patients in law enforcement custody
- Pregnancy or refusal to undergo pregnancy testing as per hospital policy before anesthesia
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Clements University Hospital
Dallas, Texas, United States, 75390
Actively Recruiting
Research Team
C
Christopher Choi
CONTACT
K
Kapil Anand
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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