Assessment of usefulness of capnographic monitoring during bronchoscopy under sedation.

Assessment of usefulness of capnographic monitoring during bronchoscopy under sedation. - Assessment of usefulness of capnographic monitoring during bronchoscopy under sedation.

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000023633

Enrollment

100

Registered

2016-08-16

Start date

2016-09-01

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

Pulmonary diseases

Interventions

Smart CapnoLine Guardian(Medtronic), Capnostream 20P (Medtronic) During bronchoscopy Normal cannula tube During bronchoscopy

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1. Patients age is more than 20 years old. 2. Patient to perform bronchoscopy 3. Informed consent for using sedatives.

Exclusion criteria

Exclusion criteria: 1. Patients undergo therapeutic bronchoscopy. 2. Patients without sedatives. 3. Patients who cannot be attached to oral device.

Design outcomes

Primary

Measure	Time frame
Comparison of total duration time under 90% in SpO2.	—

Secondary

Measure	Time frame
Comparison of median values in lowest levels of SpO2	—

Countries

Japan

Contacts

Public ContactTsukasa Ishiwata

Chiba university Department of respirology

ishiwatat@chiba-u.jp043-222-7171

Outcome results

None listed

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