Effects of Increased Tidal Volume on Internal Jugular Vein Cross-sectional Area

This study has been completed.
Sponsor:
Information provided by:
Yonsei University
ClinicalTrials.gov Identifier:
NCT01154660
First received: June 30, 2010
Last updated: April 18, 2011
Last verified: April 2011
  Purpose

As increasing tidal volume, the cross sectional area and circumference of Internal Jugular Vein (IJV) could increase. And In the previous study, Trendelenburg position can increase size of IJV. So investigators would compare the cross sectional area, circumference of IJV and peak airway pressure in neutral and Trendelenburg position


Condition Intervention
General Anesthesia
Surgery
Other: Tidal Volume

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Open Label
Official Title: Effects of Increased Tidal Volume on Internal Jugular Vein Cross-sectional Area

Further study details as provided by Yonsei University:

Enrollment: 40
Study Start Date: July 2010
Study Completion Date: December 2010
Primary Completion Date: November 2010 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: Neutral Other: Tidal Volume
observation of IJV circumference and cross sectional area using ultrasonography by changing of tidal volume
Active Comparator: Trendelenberg Other: Tidal Volume
observation of IJV circumference and cross sectional area using ultrasonography by changing of tidal volume

  Eligibility

Ages Eligible for Study:   25 Years to 75 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • patients who are undergoing general anesthesia

Exclusion Criteria:

  • history of IJV cannulation
  • uncontrolled cardiovascular disease
  • severe pulmonary problem
  • cervical spinal impairment
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01154660

Locations
Korea, Republic of
Severance Hospital, Anesthesiology & Pain Medicine
Seoul, Korea, Republic of, 120-752
Sponsors and Collaborators
Yonsei University
  More Information

No publications provided

Responsible Party: Hye-Keum Kil / Professor, Department of Anaesthesiology and Pain Medicine
ClinicalTrials.gov Identifier: NCT01154660     History of Changes
Other Study ID Numbers: 4-2009-0734
Study First Received: June 30, 2010
Last Updated: April 18, 2011
Health Authority: South Korea: Korea Food and Drug Administration (KFDA)

Keywords provided by Yonsei University:
any operation that required for general anesthesia

ClinicalTrials.gov processed this record on July 22, 2014