Usefulness of bedside portable endoscopy in diagnosis and risk stratification of gastrointestinal bleeding

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0000298

Enrollment

Registered

2011-12-22

Start date

2012-01-02

Completion date

Unknown

Last updated

2019-03-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Medical Device : The bedside portable endoscopy will be performed in patients suspicious of upper gastrointestinal bleeding following the nasogastric tube aspiration. The lesion will be confirmed by c

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Over 17 years old patients who visit emergency room for the symptoms of gastrointestinal bleeding and need upper gastrointestinal endoscopic examination

Exclusion criteria

Exclusion criteria: patients who cannot undergo upper gastrointestinal endoscopy patients who cannot take the nasogastric tube insertion patients who refuse to give the consent of the study

Design outcomes

Primary

Measure	Time frame
sensitivity and specificity of bleeding by nasogastric tube aspiration ;sensitivity and specificity of bleeding by bedside portable endoscopy	—

Secondary

Measure	Time frame
rebleeding within 1 month;mortality within 1 month	—

Countries

Korea, Republic of

Contacts

Public ContactEun Soo Kim

Keimyung University

Outcome results