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Effect of Breathing Circuits on Intraoperative Body Temperature (BT)

Seoul National University logo

Seoul National University

Status

Completed

Conditions

Brain Tumor

Treatments

Device: Group M
Device: Group C
Device: Group E

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

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

Enrollment

111 patients

Sex

All

Ages

18 to 70 years old

Volunteers

Accepts Healthy Volunteers

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

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

111 participants in 3 patient groups, including a placebo group

Group C
Placebo Comparator group
Description:
non-heated, non-humidified conventional breathing circuit was used in group C patient
Treatment:
Device: Group C
Group E
Experimental group
Description:
breathing tube which apply humidity and heat (Evaqua™ Breathing Circuits manufactured by Fischer \& Paykel)was used in group E patient
Treatment:
Device: Group E
Group M
Experimental group
Description:
Heated humid tube with a warming device (Mega Acer kit manufactured by Acemedical,Seoul Korea)was used in group M patient
Treatment:
Device: Group M

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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