The observational study on the safety of dexmedetomidine during double-balloon endoscope

The observational study on the safety of dexmedetomidine during double-balloon endoscope - The observational study on the safety of dexmedetomidine during double-balloon endoscope

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

JPRN

Registry ID

JPRN-UMIN000015785

Enrollment

250

Registered

2015-07-01

Start date

2015-07-01

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 intestine disease

Interventions

None listed

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Patients who will be performed small-bowel enteroscopy with suspected or known small bowel diseases

Exclusion criteria

Exclusion criteria: Pregnant patients Patients with poor general condition Patients with serious cardiovascular or pulmonary disease, renal dysfunction and liver dysfunction.

Design outcomes

Primary

Measure	Time frame
body movement during double-balloon endoscopy	—

Secondary

Measure	Time frame
Circulation and Respiration during double-balloon endoscopy	—

Countries

Japan

Contacts

Public ContactHiroshi Oshima

Nagoya University Graduate School of Medicine Department of Gastroenterology and Hepatology

h-oshima@med.nagoya-u.ac.jp052-744-2172

Outcome results