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

NCT ID: NCT03510013

Last Updated: 2018-08-08

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

100 participants

Study Classification

INTERVENTIONAL

Study Start Date

2018-04-01

Study Completion Date

2018-05-31

Brief Summary

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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

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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

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Anesthesia

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

All participants will receive sevoflurane 8% with O2:N2O or O2:air 1:1 L/min under controlled ventilation. Time to achieve alveolar concentration of sevoflurane of 1%, 1.5%, 2%, 2.5%, 3% and 3.5% will be recorded.
Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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1-1-8 wash-in

Wash-in using O2:N2O or O2:air 1:1 L/min with sevoflurane 8%

Group Type EXPERIMENTAL

1-1-8 wash-in

Intervention Type PROCEDURE

wash-in phase during start of low flow anesthesia

Sevoflurane

Intervention Type DRUG

Drug used for wash-in protocol

Interventions

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1-1-8 wash-in

wash-in phase during start of low flow anesthesia

Intervention Type PROCEDURE

Sevoflurane

Drug used for wash-in protocol

Intervention Type DRUG

Other Intervention Names

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Inhalation anesthetic

Eligibility Criteria

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Inclusion Criteria

* ASA classification I-II
* age 18-65 years

Exclusion Criteria

* BMI \> 35
* contraindicated for N2O
* • with pulmonary or cardiac disease
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Khon Kaen University

OTHER

Sponsor Role lead

Responsible Party

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Thepakorn Sathitkarnmanee

Associate Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Thepakorn Sathitkarnmanee, MD

Role: PRINCIPAL_INVESTIGATOR

Faculty of Medicine, Khon Kaen University

Locations

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Faculty of Medicine, Khon Kaen University

Khon Kaen, , Thailand

Site Status

Countries

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Thailand

References

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Tribuddharat S, Sathitkarnmanee T, Vattanasiriporn N, Thananun M, Nonlhaopol D, Somdee W. 1-1-8 one-step sevoflurane wash-in scheme for low-flow anesthesia: simple, rapid, and predictable induction. BMC Anesthesiol. 2020 Jan 24;20(1):23. doi: 10.1186/s12871-020-0940-2.

Reference Type DERIVED
PMID: 31980020 (View on PubMed)

Other Identifiers

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HE601228

Identifier Type: -

Identifier Source: org_study_id

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