Tolerability evaluation of newly ultrathin double-balloon endoscopy for the diagnosis and treatment of small bowel diseases: Multicenter prospective study

Tolerability evaluation of newly ultrathin double-balloon endoscopy for the diagnosis and treatment of small bowel diseases: Multicenter prospective study - Clinical utility of newly double-balloon enteroscope

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

JPRN

Registry ID

JPRN-UMIN000015836

Enrollment

100

Registered

2015-03-01

Start date

2015-07-21

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 bowel disease

Interventions

None listed

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1age: 20 or more than 20 years old 2obtained informed consent 3oral route of double-balloon endoscopy planned for the suspected small bowel diseases

Exclusion criteria

Exclusion criteria: 1)Patients with acute abdomen 2)Patients with severe acute inflammation 3)pregnant patients 4)Patients in a very bad general condition 5)Patients having severe blood clotting defect 6Patients who have participated in same clinical trials. 7Patients, the investigator (or the subinvestigator) considers, inappropriate for entry into the trial.

Design outcomes

Primary

Measure	Time frame
difference of serum amylase level between before and after procedure	—

Countries

Japan

Contacts

Public ContactMasanao Nakamura

Nagoya University Graduate School of Medicine Department of Gastroenterology and Hepatology

makamura@med.nagoya-u.ac.jp052-744-2172

Outcome results