A Bedside Portable Endoscopy for the Esophageal Foreign Body

Esophageal Foreign Body Clinical Trial

Official title:

Efficacy of a Bedside Portable Endoscopy on Identifying the Esophageal Foreign Body

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03009383
• Other study ID #: KNUH20161227
• Status: Completed
• Phase: N/A
• Start date: October 2016
• Est. completion date: December 2017

Study information

• Verified date: July 2018
• Source: Kyungpook National University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to determine whether a bedside portable endoscopy is effective in identifying the esophageal foreign body in the emergency room.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 27
• Est. completion date: December 2017
• Est. primary completion date: October 2017
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 85 Years

Eligibility

Inclusion Criteria:

• Patients who visit the emergency room due to apparent foreign body in esophagus

Exclusion Criteria:

• Patients unable to insert a portable endoscopy through the nasal cavity

• Patients unable to undergo conventional esophagogastroduodenoscopy for a gold standard examination

Related Conditions & MeSH terms

• Esophageal Foreign Body
• Foreign Bodies

Intervention

Device:
• A bedside portable endoscopy

Locations

Country	Name	City	State
Korea, Republic of	Kyungpook National University Hospital	Daegu

Sponsors (1)

Lead Sponsor	Collaborator
Kyungpook National University

Country where clinical trial is conducted

Korea, Republic of, 

References & Publications (1)

Choi JH, Choi JH, Lee YJ, Lee HK, Choi WY, Kim ES, Park KS, Cho KB, Jang BK, Chung WJ, Hwang JS. Comparison of a novel bedside portable endoscopy device with nasogastric aspiration for identifying upper gastrointestinal bleeding. World J Gastroenterol. 20 — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Sensitivity, specificity, positive predictive value and negative predictive value of the bedside portable endoscopy to identify esophageal foreign body defined by comparison with conventional esophagogastroduodenoscopy as a gold standard method		Within 1 hr after procedure