A prospective study of the optimal depth of anesthesia for remimazolam anesthesia

A prospective study of the optimal depth of anesthesia for remimazolam anesthesia - A prospective study on the depth of anesthesia for remimazolam anesthesia

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

JPRN

Registry ID

JPRN-UMIN000044418

Enrollment

Registered

2021-06-03

Start date

2021-07-01

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

Not specified

Interventions

None listed

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Eligibility criteria are patients who meet the following conditions. (1) Patients scheduled for general anesthesia surgery with spinal subarachnoid anesthesia at Tohoku University Hospital (2) Adult patients aged 20 years or older (3) Gender is not required.

Exclusion criteria

Exclusion criteria: (1) Pregnant and lactating women (2) Patients with Child-Pugh classification C or higher (3) Patients with central nervous system diseases and psychiatric diseases (4) Patients who regularly use CNS-acting drugs (5) Heavy drinkers of alcohol and illegal drugs (6) Patients who cannot communicate in Japanese (7) Patients who had an adverse reaction to remimazolam and required a change in anesthetic (8) Patients who could not be awakened from anesthesia and extubated in the operating room immediately after the completion of surgery

Design outcomes

Primary

Measure	Time frame
EEG changes during remimazolam anesthesia	—

Secondary

Measure	Time frame
The validity of a commercially available depth of anesthesia monitor	—

Countries

Japan

Contacts

Public ContactKOTOE KAMATA

Tohoku University School of Medicine Department of Anesthesiology and Perioperative Medicine

kotoe.kamata.c3@tohoku.ac.jp+81-22-717-7321

Outcome results