Effect of Breathing Circuits on Intraoperative Body Temperature

NCT ID: NCT01831843

Last Updated: 2013-09-17

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

111 participants

Study Classification

INTERVENTIONAL

Study Start Date

2013-01-31

Study Completion Date

2013-07-31

Brief Summary

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To evaluate differences in intraoperative body temperature between heated huimid breathing circuit and conventional breathing circuit

Detailed Description

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Conditions

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Brain Tumor

Keywords

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core body temperature humidity circuit temperature

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

SINGLE

Participants

Study Groups

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Group C

non-heated, non-humidified conventional breathing circuit was used in group C patient

Group Type PLACEBO_COMPARATOR

Group C

Intervention Type DEVICE

non-heated, non-humidified conventional breathing circuit was used in group C patient

Group E

breathing tube which apply humidity and heat (Evaqua™ Breathing Circuits manufactured by Fischer \& Paykel)was used in group E patient

Group Type EXPERIMENTAL

Group E

Intervention Type DEVICE

breathing tube which apply humidity and heat (Evaqua™ Breathing Circuits manufactured by Fischer \& Paykel)was used in group E patient

Group M

Heated humid tube with a warming device (Mega Acer kit manufactured by Acemedical,Seoul Korea)was used in group M patient

Group Type EXPERIMENTAL

Group M

Intervention Type DEVICE

Heated humid tube with a warming device (Mega Acer kit manufactured by Acemedical,Seoul Korea)was used in group M patient

Interventions

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Group C

non-heated, non-humidified conventional breathing circuit was used in group C patient

Intervention Type DEVICE

Group E

breathing tube which apply humidity and heat (Evaqua™ Breathing Circuits manufactured by Fischer \& Paykel)was used in group E patient

Intervention Type DEVICE

Group M

Heated humid tube with a warming device (Mega Acer kit manufactured by Acemedical,Seoul Korea)was used in group M patient

Intervention Type DEVICE

Other Intervention Names

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conventional circuit Evaqua™ Breathing Circuits manufactured by Fischer & Paykel Mega Acer kit manufactured by Acemedical,Seoul Korea

Eligibility Criteria

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Inclusion Criteria

* aged 18-70 years,
* ASA I or II
* patients scheduled for craniotomy under general anesthesia

Exclusion Criteria

* ASA III or IV
* Duration of anesthesia time less than 4 hours
* emergency operation
Minimum Eligible Age

18 Years

Maximum Eligible Age

70 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Seoul National University Hospital

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Seoul National University Hospital

Seoul, Seoul, South Korea

Site Status

Countries

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South Korea

References

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Kim E, Lee SY, Lim YJ, Choi JY, Jeon YT, Hwang JW, Park HP. Effect of a new heated and humidified breathing circuit with a fluid-warming device on intraoperative core temperature: a prospective randomized study. J Anesth. 2015 Aug;29(4):499-507. doi: 10.1007/s00540-015-1994-z. Epub 2015 Mar 14.

Reference Type DERIVED
PMID: 25771760 (View on PubMed)

Other Identifiers

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php2

Identifier Type: -

Identifier Source: org_study_id