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

NCT ID: NCT01054378

Last Updated: 2010-12-07

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE4

Total Enrollment

43 participants

Study Classification

INTERVENTIONAL

Study Start Date

2010-01-31

Study Completion Date

2010-04-30

Brief Summary

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

Detailed Description

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Conditions

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

Study Design

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Primary Study Purpose

TREATMENT

Interventions

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M-mode ultrasonography

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

Intervention Type PROCEDURE

Eligibility Criteria

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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
Minimum Eligible Age

20 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Yonsei University

OTHER

Sponsor Role lead

Responsible Party

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Yonsei University College of Medicine, Seoul, South Korea,

Principal Investigators

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Duck Mi Yoon

Role: PRINCIPAL_INVESTIGATOR

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

Locations

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Severance Hospital, Yonsei University College of Medicine

Seoul, , South Korea

Site Status

Countries

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South Korea

Other Identifiers

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4-2009-0614

Identifier Type: -

Identifier Source: org_study_id