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Accuracy Assessment of Exhaled Propofol Concentration Monitoring in Patients under General Anesthesia

Accuracy Assessment of Exhaled Propofol Concentration Monitoring in Patients under General Anesthesia - Assessment of Exhaled Propofol Monitor

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000036435
Enrollment
40
Registered
2019-04-07
Start date
2019-04-08
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

Patient Undergoing Elective Surgery under General Anesthesia

Interventions

Propofol will be administered using target-controlled infusion. The target concentration is controlled between 3 to 6 mcg/ml during the induction of anesthesia, and 2 to 5 mcg/ml during maintenance of

Sponsors

Showa University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patient undergoing elective surgery under general anesthesia (20 patients aged 20 to 64, and 20 patients aged 65 or older)

Exclusion criteria

Exclusion criteria: (1) Contraindication to propofol or hydroxyethil starch administration (2) Obstructive and/or restrictive ventilatory impairment (3) American Society of Anesthesiologists physical status 4 or larger

Design outcomes

Primary

MeasureTime frame
Ratio of exhaled propofol cocentration versus plasma propofol concentration or an index simialr to the ratio during the general anesthesia

Secondary

MeasureTime frame
1. Ratio of measured propofol cocentration versus predicted plasma propofol concentration or an index simialr to the ratio during the general anesthesia 2. pharmacokinetic model to predict plasmaconcentration using exhaled propofol concentration

Countries

Japan

Contacts

Public ContactKenichi Masui

Showa University School of Medicine Department of Anesthesiology

kenichi@masuinet.com03-3784-8575

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026