Clinical comparison of two anesthetic depth monitors; Noxious Stimulation Response Index(NSRI) versus BIS

Clinical comparison of two anesthetic depth monitors; Noxious Stimulation Response Index(NSRI) versus BIS - Clinical comparison of two anesthetic depth monitors

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

JPRN

Registry ID

JPRN-UMIN000019633

Enrollment

Registered

2015-11-04

Start date

2015-11-05

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

Patients undergoing elective surgery under general anesthesia

Interventions

None listed

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Patients who are ASA 1 or 2 undergoing elective surgery under general anesthesia with tracheal intubation. (150cm<=height<=200cm, 40kg<=body weight<=140kg)

Exclusion criteria

Exclusion criteria: Patients who are ASA 3 or more Emergency surgery General anesthesia with local anesthesia Liver dysfunction Renal dysfunction Central nervous system disease

Design outcomes

Primary

Measure	Time frame
Correlation between NSRI and BIS	—

Countries

Japan

Contacts

Public ContactKenichiro Koda

Toho University Sakura medical center Department of anesthesiology

kenich-kou@sakura.med.toho-u.ac.jp043-462-8811

Outcome results