Comparison of the performance between forward view and oblique view EUS

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

CRIS

Registry ID

KCT0001000

Enrollment

Registered

2014-02-06

Start date

2012-12-03

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 : Patients were placed in a left lateral decubitus position and all EUS procedures were performed under conscious sedation with intravenous midazolam and propofol according to the judgm

Olympus Medical System, Tokyo, Japan) and the newly developed FV-EUS (GIF-Y-0007-UCT

Olympus Medical System, Tokyo, Japan) were used. The sequence in which these techniques were employed was randomly assigned. For the study protocol, two groups were formed depending on the experience

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: pancreaticobiliary diseases of unknown etiology (20-89 year-old) were prospectively enrolled in the study.

Exclusion criteria

Exclusion criteria: The exclusion criteria were as follows: pregnancy, bleeding tendency (prothrombin time INR > 1.5 or platelet < 80,000/µL), and critically ill patients.

Design outcomes

Primary

Measure	Time frame
Quality of visualization of forward view EUS compared with Oblique view EUS	—

Secondary

Measure	Time frame
Visualization time ;quality of EUS-FNA	—

Countries

Korea, Republic of

Contacts

Public ContactSeohyun Lee

Asan Medical Center

Outcome results