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

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT01054378
First Posted: January 22, 2010
Last Update Posted: December 7, 2010
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by:
Yonsei University
  Purpose
The temporary diaphrgmatic dysfunction will occur after stellate ganglion block(SGB) and will be easily detected by M-mode ultrasonography

Condition Intervention Phase
Head Pain Neck Pain Shoulder Pain Arm Pain Neural Sensory Hearing Loss Procedure: M-mode ultrasonography Phase 4

Study Type: Interventional
Study Design: Primary Purpose: Treatment

Resource links provided by NLM:


Further study details as provided by Yonsei University:

Primary Outcome Measures:
  • 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. ]

Enrollment: 43
Study Start Date: January 2010
Study Completion Date: April 2010
Primary Completion Date: March 2010 (Final data collection date for primary outcome measure)
Intervention Details:
    Procedure: M-mode ultrasonography
    Evaluation of diaphragmatic movement using M-mode ultrasonography before and after stellate ganglion block with 1% lidocaine
  Eligibility

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Ages Eligible for Study:   20 Years to 65 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

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
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01054378


Locations
Korea, Republic of
Severance Hospital, Yonsei University College of Medicine
Seoul, Korea, Republic of
Sponsors and Collaborators
Yonsei University
Investigators
Principal Investigator: Duck Mi Yoon Department of Anesthesiology and Pain Medicine, Yonsei University College of Medicine, Seoul, Korea
  More Information

Responsible Party: Duck Mi Yoon/Professor of Anesthesiology and Pain Medicine,, Yonsei University College of Medicine, Seoul, South Korea,
ClinicalTrials.gov Identifier: NCT01054378     History of Changes
Other Study ID Numbers: 4-2009-0614
First Submitted: January 21, 2010
First Posted: January 22, 2010
Last Update Posted: December 7, 2010
Last Verified: December 2010

Additional relevant MeSH terms:
Neck Pain
Hearing Loss
Shoulder Pain
Hearing Loss, Sensorineural
Pain
Neurologic Manifestations
Nervous System Diseases
Signs and Symptoms
Hearing Disorders
Ear Diseases
Otorhinolaryngologic Diseases
Sensation Disorders
Arthralgia
Joint Diseases
Musculoskeletal Diseases