Effects of Shoulder Edema on Intubated Tube in Patients Undergoing Shoulder Arthroscopy

August 29, 2016 updated by: Sira Bang, Inje University
Intubation is needed in general anesthesia and appropriate cuff pressure is important to avoid trauma or postoperative sore throat and aspiration. Shoulder arthroscope uses some amount of irrigation fluid and it can influence to cuff pressure. Therefore, we will measure cuff pressure during shoulder arthroscope.

Study Overview

Status

Completed

Conditions

Study Type

Observational

Enrollment (Actual)

40

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

  • Korea, Republic of
    • Jung-Gu
      • Seoul, Jung-Gu, Korea, Republic of, 100-032
        • Inje University Seoul Paik Hospital, Seoul, Korea

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

20 years to 65 years (ADULT, OLDER_ADULT)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Probability Sample

Study Population

Patints who undergoing shoulder arthroscopy American Society of Anesthesiologists (ASA) 1,2

Description

Inclusion Criteria:

  • American Society of Anesthesiologists (ASA) 1,2 Age 20-65

Exclusion Criteria:

  • emergency operation anticipated difficult intubation chronic obstructive lung disease recent upper respiratory infection

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

Cohorts and Interventions

Group / Cohort
shoulder arthroscopy

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Direct intracuff pressure measurement technique using manometer
Time Frame: every one hour during operarion
every one hour during operarion

Collaborators and Investigators

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

Sponsor

Inje University

Collaborators

Fresenius Kabi Korea

Investigators

  • Principal Investigator: Sira Bang, MD, PhD, Inje University Seoul Paik Hospital, Seoul, Korea

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

June 1, 2014

Primary Completion (Actual)

July 1, 2016

Study Completion (Actual)

July 1, 2016

Study Registration Dates

First Submitted

July 3, 2014

First Submitted That Met QC Criteria

July 8, 2014

First Posted (Estimate)

July 9, 2014

Study Record Updates

Last Update Posted (Estimate)

August 31, 2016

Last Update Submitted That Met QC Criteria

August 29, 2016

Last Verified

August 1, 2016

More Information

Terms related to this study

Other Study ID Numbers

  • IIT-2014-192

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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