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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03270696
Other study ID # JHSeo_MV
Secondary ID
Status Completed
Phase N/A
First received August 23, 2017
Last updated April 11, 2018
Start date August 23, 2017
Est. completion date January 30, 2018

Study information

Verified date September 2017
Source Seoul National University Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study is conducted to evaluate the efficacy of simultaneous injection of propofol and rocuronium in inducing general anesthesia.


Recruitment information / eligibility

Status Completed
Enrollment 114
Est. completion date January 30, 2018
Est. primary completion date January 30, 2018
Accepts healthy volunteers No
Gender All
Age group 20 Years and older
Eligibility Inclusion Criteria:

- patients undergoing elective surgery requiring endotracheal intubation

- ASA I, II, and III

- above 20 years

Exclusion Criteria:

- refuse to enroll

- patients with risk of aspirating gastric contents

- patients in whom NMBs are contraindicated

- patients with predictors of difficult mask ventilation

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
administration of propofol and rocuronium
compare the tidal volume applied from starting facemask ventilation under 15cmH2O of PCV for 1 minute according to administrating propofol and rocuronium simultaneously, or ordinally

Locations

Country Name City State
Korea, Republic of Seoul National University Hospital Seoul

Sponsors (1)

Lead Sponsor Collaborator
Seoul National University Hospital

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary mean tidal volume mean tidal volume of facemask ventilation in 1 minute from starting facemask ventilation for 1 minute
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