Diaphragmatic Movement Before and After Stellate Ganglion Block : A Ultrasonographic Study

This study has been completed.

Sponsor:

Information provided by:

Yonsei University

ClinicalTrials.gov Identifier:

NCT01054378

First received: January 21, 2010

Last updated: December 6, 2010

Last verified: December 2010

History of Changes

Tracking Information

First Received Date ^ICMJE

January 21, 2010

Last Updated Date

December 6, 2010

Start Date ^ICMJE

January 2010

Primary Completion Date

March 2010 (final data collection date for primary outcome measure)

Current Primary Outcome Measures ^ICMJE

The amplitude of diaphragm movement before and after SGB during quiet breathing, deep breathing and voluntary sniff, inspiratory time and expiratory time, oxygen saturation [ Time Frame: The ultrasonographic evaluation will take place just before and 30 minutes after stellate ganglion block. ] [ Designated as safety issue: No ]

Original Primary Outcome Measures ^ICMJE

The amplitude of diaphragm movement before and after SGB during quiet breathing, deep breathing and voluntary sniff, inspiratory time and expiratory time, oxygen saturaion [ Time Frame: The ultrasonographic evaluation will take place just before and 30 minutes after stellate ganglion block. ] [ Designated as safety issue: No ]

Change History

Complete list of historical versions of study NCT01054378 on ClinicalTrials.gov Archive Site

Current Secondary Outcome Measures ^ICMJE

Not Provided

Original Secondary Outcome Measures ^ICMJE

Not Provided

Current Other Outcome Measures ^ICMJE

Not Provided

Original Other Outcome Measures ^ICMJE

Not Provided

Descriptive Information

Brief Title ^ICMJE

Diaphragmatic Movement Before and After Stellate Ganglion Block : A Ultrasonographic Study

Official Title ^ICMJE

Not Provided

Brief Summary

The temporary diaphrgmatic dysfunction will occur after stellate ganglion block(SGB) and will be easily detected by M-mode ultrasonography

Detailed Description

Not Provided

Study Type ^ICMJE

Interventional

Study Phase

Phase 4

Study Design ^ICMJE

Primary Purpose: Treatment

Condition ^ICMJE

Head Pain
Neck Pain
Shoulder Pain
Arm Pain
Neural Sensory Hearing Loss

Intervention ^ICMJE

Procedure: M-mode ultrasonography

Evaluation of diaphragmatic movement using M-mode ultrasonography before and after stellate ganglion block with 1% lidocaine

Study Arm (s)

Not Provided

Publications *

Not Provided

* Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.

Recruitment Information

Recruitment Status ^ICMJE

Completed

Enrollment ^ICMJE

Completion Date

April 2010

Primary Completion Date

March 2010 (final data collection date for primary outcome measure)

Eligibility Criteria ^ICMJE

Inclusion Criteria:

ASA class I-II patients who have head and neck pain or shoulder pain or sudden sensory neural hearing loss

Exclusion Criteria:

coagulopathy, pulmonary disease, neuropathy

Gender

Both

Ages

20 Years to 65 Years

Accepts Healthy Volunteers

Contacts ^ICMJE

Contact information is only displayed when the study is recruiting subjects

Location Countries ^ICMJE

Korea, Republic of

Administrative Information

NCT Number ^ICMJE

NCT01054378

Other Study ID Numbers ^ICMJE

4-2009-0614

Has Data Monitoring Committee

Not Provided

Responsible Party

Duck Mi Yoon/Professor of Anesthesiology and Pain Medicine,, Yonsei University College of Medicine, Seoul, South Korea,

Study Sponsor ^ICMJE

Yonsei University

Collaborators ^ICMJE

Not Provided

Investigators ^ICMJE

Principal Investigator:

Duck Mi Yoon

Department of Anesthesiology and Pain Medicine, Yonsei University College of Medicine, Seoul, Korea

Information Provided By

Yonsei University

Verification Date

December 2010

^ICMJE Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP

To Top