Clinical Trials Directory

Trials / Completed

CompletedNCT03510013

1-1-8 Wash-in for Sevoflurane Low Flow Anesthesia

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
100 (actual)
Sponsor
Khon Kaen University · Academic / Other
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Accepted

Summary

The investigators propose a new wash-in technique for sevoflurane low flow anesthesia with fresh gas flow of O2:N2O or O2:air 1:1 L/min with sevoflurane 8%. The objective of this study is to identify time to achieve alveolar concentration of sevoflurane at 1, 1.5, 2, 2.5, 3, and 3.5%

Detailed description

The benefits of low flow anesthesia are economic, less pollution, more heat and humidity preservation but it requires appropriate wash-in phase. The current wash-in protocols for sevoflurane are complicated and time consuming. The investigators propose a new 1-1-8 sevoflurane wash-in protocol which is more simple and predictable. The objective of this study is to identify time to achieve alveolar concentration of sevoflurane at 1, 1.5, 2, 2.5, 3, and 3.5% with 1-1-8 wash-in protocol. All patients will receive iv propofol 2 mg/kg as induction agent and succinyl choline 1.5 mg/kg for intubation. Then the ventilation will be controlled to achieve end-tidal CO2 30-35 mmHg with O2:N2O or O2:air 1:1 L/min with sevoflurane 8%. Time to achieve alveolar concentration of sevoflurane at 1, 1.5, 2, 2.5, 3, and 3.5% will be recorded and analyzed. After that, the concentration of sevoflurane and anesthetic technique will be adjusted to requirement of anesthesiologist.

Conditions

Interventions

TypeNameDescription
PROCEDURE1-1-8 wash-inwash-in phase during start of low flow anesthesia
DRUGSevofluraneDrug used for wash-in protocol

Timeline

Start date
2018-04-01
Primary completion
2018-05-31
Completion
2018-05-31
First posted
2018-04-27
Last updated
2018-08-08

Locations

1 site across 1 country: Thailand

Source: ClinicalTrials.gov record NCT03510013. Inclusion in this directory is not an endorsement.