JACE appropriate use survey for patency capsule study

JACE appropriate use survey for patency capsule study - J-POP Study

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

JPRN

Registry ID

JPRN-UMIN000010513

Enrollment

1000

Registered

2013-04-17

Start date

2013-01-01

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

The patients who performed patency capsule in the research cooperation institutions.

Interventions

None listed

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: The patients who performed patency capsule in the research cooperation institutions.

Exclusion criteria

Exclusion criteria: The patients who were had allergy for barium. The patients who were judged as inadequate by the physician.

Design outcomes

Primary

Measure	Time frame
To investigate the clinical backgrounds and contents of examination in patients who were performed patency capsule. (primary survey)	—

Secondary

Measure	Time frame
To evaluate the efficacies and issues of patency capsule and following capsule endoscopy for the medical practice in patients with Crohns disease. (for patients in primary survey) To evaluate adverse events for patency capsule precisely. (for patients in additional survey in addition to primary survey)	—

Countries

Japan

Contacts

Public ContactKenji Watanabe

Osaka City University Graduate School of Medicine Department of Gastroenterology

kenjiw1779@gmail.com06-6645-3811

Outcome results