A Modeling of Changes in Tidal Volume With Concentration of Inhalational Anesthetics

April 6, 2018 updated by: Hee-Soo Kim, Seoul National University Hospital

A Modeling of Changes in Tidal Volume With Concentration of Inhalational Anesthetics Under General Anesthesia Using Laryngeal Mask Airway

modelling of tidal volume with inhalational anesthetic concentration

Study Overview

Status

Completed

Conditions

Detailed Description

The investigators would like to develop the modelling of tidal volume with inhalational anesthetic concentration during spontaneous breathing during general anesthesia in children

Study Type

Observational

Enrollment (Actual)

50

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

No older than 12 years (Child)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

children under general anesthesia

Description

Inclusion Criteria:

- general anesthesia

Exclusion Criteria:

-

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Observational Models: Case-Only
  • Time Perspectives: Retrospective

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
concentration
Time Frame: 20 minutes
inhalational anesthetic concentration
20 minutes

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Seoul National University Hospital

Investigators

  • Principal Investigator: Hee-Soo Kim, MD, Seoul National University Hospital

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

February 21, 2017

Primary Completion (Actual)

March 1, 2018

Study Completion (Actual)

March 20, 2018

Study Registration Dates

First Submitted

April 1, 2018

First Submitted That Met QC Criteria

April 1, 2018

First Posted (Actual)

April 9, 2018

Study Record Updates

Last Update Posted (Actual)

April 10, 2018

Last Update Submitted That Met QC Criteria

April 6, 2018

Last Verified

April 1, 2018

More Information

Terms related to this study

Other Study ID Numbers

  • 1803-068-929

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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