Randomized Controlled Trial to Compare the Insertability between Conventional Single Balloon Enteroscope versus Newly Developed Single Balloon Enteroscpe equipped with Passive Bending and High Force Transmission Insertion Tube.

Randomized Controlled Trial to Compare the Insertability between Conventional Single Balloon Enteroscope versus Newly Developed Single Balloon Enteroscpe equipped with Passive Bending and High Force Transmission Insertion Tube. - Randomized Controlled Trial to Compare the Insertability between Conventional Single Balloon Enteroscope versus Newly Developed Single Balloon Enteroscpe equipped with Passive Bending and High Force Transmission Insertion Tube.

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000007851

Enrollment

Registered

2012-05-01

Start date

2012-05-01

Completion date

Unknown

Last updated

2026-06-29

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

Conditions

Small intestinal abmormalities

Interventions

Conventional Single Balloon Enteroscope Newly Developed Single Balloon Enteroscpe equipped with Passive Bending and High Force Transmission Insertion Tube.

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Patients required investigation by using retrograde enteroscope.

Exclusion criteria

Exclusion criteria: 1)Post ileocecal resection. 2)Cecal valve Stenosis. 3)Severe inflammation in ileocecal area.

Design outcomes

Primary

Measure	Time frame
Passing time from cecal valve to the terminal ileum	—

Countries

Japan

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026