Actively Recruiting

Age: 18Years +
All Genders
Healthy Volunteers
NCT06507670

Point of Care Ultrasound for the Detection of Esophageal Food Bolus

Led by WellSpan Health · Updated on 2024-07-18

30

Participants Needed

1

Research Sites

130 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

Point of Care Ultrasound for the Detection of Esophageal Food Bolus

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 years or older
  • For case group: signs and symptoms of esophageal food bolus or foreign body
  • For control group: no signs or symptoms of esophageal food bolus or foreign body
  • For control group: age and sex matched to a previously enrolled case subject
Not Eligible

You will not qualify if you...

  • Prior esophageal surgery
  • History of head or neck cancer
  • Incarcerated individuals
  • Unable to provide consent
  • Clinical instability or airway compromise
  • For control group: presence of nausea, vomiting, diarrhea, abdominal pain, chest pain, shortness of breath, difficulty swallowing or pain when swallowing, or cough

AI-Screening

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Trial Site Locations

Total: 1 location

1

WellSpan Health York Hospital

York, Pennsylvania, United States, 17403

Actively Recruiting

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Research Team

K

Kristen Oliff

CONTACT

B

Brent Becker, MD

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

2

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