RECRUITING

Point of Care Ultrasound for the Detection of Esophageal Food Bolus

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

This will be a prospective, observational, case-control study of adult patients presenting to the WellSpan York Hospital Emergency Department (YHED) with signs and symptoms of esophageal food or foreign body impaction. Point of care ultrasound (POCUS) will then be performed by a trained emergency physician to collect ultrasound data, including the presence or absence of direct visualization food bolus/foreign body, as well as secondary markers of dilatation, such as maximal esophageal area. Investigators will also enroll an age/sex-matched control group of asymptomatic individuals to establish baseline esophageal measurements. Patients will otherwise receive medical treatment per standard of care. Subsequent interventions will also be documented, including glucagon, carbonated beverages, and esophagogastroduodenoscopy (EGD). If patients remain in the ED and improve without need for EGD they will undergo repeat ultrasound. Chart review at 1 month will be performed to establish results of EGD including improvement, recurrence, or presence of pathologic abnormalities. The investigators aim to establish normal and abnormal parameters to aid in the diagnosis of esophageal food impactions to predict need for definitive EGD management.

Official Title

Point of Care Ultrasound for the Detection of Esophageal Food Bolus

Quick Facts

Study Start:2024-07-01
Study Completion:2027-01-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06507670

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:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. 1. Age ≥18 years
  2. 2. Signs and symptoms of esophageal food bolus or foreign body
  3. *
  1. 1. Prior esophageal surgery
  2. 2. History of head/neck cancer
  3. 3. Incarcerated individuals
  4. 4. Individuals unable to provide consent
  5. 5. Clinical instability or airway compromise
  6. *

Contacts and Locations

Study Contact

Kristen Oliff
CONTACT
717-851-5075
koliff@wellspan.org
Brent Becker, MD
CONTACT
717-851-4819
bbecker2@wellspan.org

Study Locations (Sites)

WellSpan Health York Hospital
York, Pennsylvania, 17403
United States

Collaborators and Investigators

Sponsor: WellSpan Health

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 Date2024-07-01
Study Completion Date2027-01-01

Study Record Updates

Study Start Date2024-07-01
Study Completion Date2027-01-01

Terms related to this study

Additional Relevant MeSH Terms

  • Esophageal Foreign Body
  • Esophageal Obstruction