The Predictive Performance of Target Effect-site Concentration controlled Infusion Pump (PION TCI®) for Microemulsion Propofol

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0000200

Enrollment

Registered

2011-10-11

Start date

2011-06-21

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

Medical Device : Aquafol infusion was started with a target effect concentration of 1 µg/ml. Anesthesia was maintained with a target effect concentration of aquafol (2-6 µg/ml) and a target-controlled

1) time to loss of consciousness, 2) 20 min after modulation of a target effect concentration of aquafol, 3) time to recovery of consciousness.

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1. American Society of Anesthesiologists Physical Status 1 or 2 2. 19-65 years 3. Patinets undergoning general anesthesia

Exclusion criteria

Exclusion criteria: 1. Abnormal laboratory results with clinical significance. 2. History of hypersensitivity to propofol

Design outcomes

Primary

Measure	Time frame
Predicitve performance	—

Secondary

Measure	Time frame
adverse event	—

Countries

Korea, Republic of

Contacts

Public ContactByung Choi

Asan Medical Center

byungmoonchoi7@gmail.com+82-2-3010-1704

Outcome results