RECRUITING

Resuscitative TEE Collaborative Registry

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

Evaluation of the Clinical Impact and Safety of Focused Transesophageal Echocardiography During Resuscitation of Critically Ill Patients in the Emergency Department and Intensive Care Settings

Quick Facts

Study Start:2020-12-01
Study Completion:2024-12-15
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT04972526

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Not specified
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Adult critically-ill patients who as part of their routine clinical care receive focused TEE in the emergency department of intensive care setting.
  1. * Children (age under 18 years)
  2. * Vulnerable populations

Contacts and Locations

Study Contact

Aarthi Kaviyarasu, BS
CONTACT
614-906-4711
aarthi.kaviyarasu@pennmedicine.upenn.edu

Principal Investigator

Felipe Teran, MD, MSCE
STUDY_CHAIR
Weill Medical College of Cornell University
Benjamin Abella, MD, MPhil
STUDY_DIRECTOR
University of Pennsylvania

Study Locations (Sites)

University of Pennsylvania
Philadelphia, Pennsylvania, 19104
United States

Collaborators and Investigators

Sponsor: University of Pennsylvania

  • Felipe Teran, MD, MSCE, STUDY_CHAIR, Weill Medical College of Cornell University
  • Benjamin Abella, MD, MPhil, STUDY_DIRECTOR, University of Pennsylvania

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2020-12-01
Study Completion Date2024-12-15

Study Record Updates

Study Start Date2020-12-01
Study Completion Date2024-12-15

Terms related to this study

Keywords Provided by Researchers

  • Transesophageal Echocardiography
  • Resuscitation
  • Cardiac Arrest
  • Point-of-care Ultrasound
  • Focused Cardiac Ultrasound

Additional Relevant MeSH Terms

  • Cardiac Arrest
  • Cardiac Arrest Circulatory
  • Cardiac Arrest, Out-Of-Hospital
  • Shock
  • Hemodynamic Instability