Investigation of factors associated with adverse events during sedation with nerve block

Investigation of factors associated with adverse events during sedation with nerve block - Investigation of factors associated with adverse events during sedation with nerve block

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

JPRN

Registry ID

JPRN-UMIN000039801

Enrollment

500

Registered

2020-03-13

Start date

2019-03-29

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

Peripheral Arterial Disease

Interventions

None listed

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Patients who underwent bypass surgery by peripheral artery disease were enrolled.

Exclusion criteria

Exclusion criteria: Refusal to participate

Design outcomes

Primary

Measure	Time frame
The ratio of occurrence of hypoxia	—

Secondary

Measure	Time frame
Operating time, anesthesia time, respiratory complications, neurological complications, renal complication, arterial partial pressure of oxygen, arterial partial pressure of carbon dioxide, oxygen saturation, length of ICU stay, length of hospital stay, level of pain	—

Countries

Japan

Contacts

Public ContactYoshiko Onodera

Asahikawa Medical University Hospital Surgical Operation Department

yonodera@asahikawa-med.ac.jp0166-68-2583

Outcome results