Actively Recruiting
Resuscitative TEE Collaborative Registry
Led by University of Pennsylvania · Updated on 2026-01-14
1000
Participants Needed
1
Research Sites
367 weeks
Total Duration
On this page
Sponsors
U
University of Pennsylvania
Lead Sponsor
W
Weill Medical College of Cornell University
Collaborating Sponsor
AI-Summary
What this Trial Is About
The general objective of this study is to evaluate the clinical impact and safety of focused, point-of-care transesophageal echocardiography (TEE) used during the evaluation of critically-ill patients in the emergency and intensive care settings. The target population for this study are critically-ill patients over the age of 18 who as part of their routine clinical care are receiving a focused TEE. The primary objective of this study is to determine the clinical impact and safety of TEE performed during the evaluation of critically-ill patients in the emergency department and intensive care settings. The secondary objective(s) of this study are to characterize the use of this imaging modality in the subsets of critically-ill patients in shock and cardiac arrest; including but not limited to; description of the frequency of studies, clinical indications, clinician characteristics, echocardiography findings, timing of studies, procedure-related complications and patient outcomes.
CONDITIONS
Official Title
Resuscitative TEE Collaborative Registry
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adult critically-ill patients who as part of their routine clinical care receive focused TEE in the emergency department or intensive care setting.
You will not qualify if you...
- Children under 18 years of age
- Vulnerable populations
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
University of Pennsylvania
Philadelphia, Pennsylvania, United States, 19104
Actively Recruiting
Research Team
C
Caleb Suh
CONTACT
F
Felipe Teran, MD, MSCE
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
5
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