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Assessment of Phase Lag Entropy(PLE) monitor for the sedation levels using propofol

Assessment of Phase Lag Entropy(PLE) monitor for the sedation levels using propofol in upper limb surgery patients under brachial plexus block

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
CRIS
Registry ID
KCT0002542
Enrollment
30
Registered
2017-11-17
Start date
2017-07-12
Completion date
Unknown
Last updated
2019-03-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

None listed

Sponsors

Soon Chun Hyang University Hospital Seoul
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: adult patients ( >18 yr old) who undergoing upper arm surgery under brachial plexus block using ultrasonogram Healthy patient who is American Society of Anesthesiology (ASA) physical status 1or 2.

Exclusion criteria

Exclusion criteria: -patient who has CNS disease, past history of CNS disease, and neurological disorder - patient who has been taken anticonvulsant agent, sedatives, analgesics, and hypnotics . - significant hepatic disease or renal disease - obesity (BMI>30) _ Obstructive sleep apnea - hypersensitivity to propofol or local anesthetics - hypersensitivity to bean or peanut _ pregnant woman

Design outcomes

Primary

MeasureTime frame
correlation of OAA/S Scale and PLE—

Secondary

MeasureTime frame
comparison PLE with BIS—

Countries

Korea, Republic of

Contacts

Public ContactSoon Im Kim

Soon Chun Hyang University

anesikim@gmail.com+82-2-709-9294

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026