Neck Pain Clinical Trial
Verified date | December 2010 |
Source | Yonsei University |
Contact | n/a |
Is FDA regulated | No |
Health authority | Korea: Food and Drug Administration |
Study type | Interventional |
The temporary diaphrgmatic dysfunction will occur after stellate ganglion block(SGB) and will be easily detected by M-mode ultrasonography
Status | Completed |
Enrollment | 43 |
Est. completion date | April 2010 |
Est. primary completion date | March 2010 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 20 Years to 65 Years |
Eligibility |
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 |
Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
Korea, Republic of | Severance Hospital, Yonsei University College of Medicine | Seoul |
Lead Sponsor | Collaborator |
---|---|
Yonsei University |
Korea, Republic of,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | The amplitude of diaphragm movement before and after SGB during quiet breathing, deep breathing and voluntary sniff, inspiratory time and expiratory time, oxygen saturation | The ultrasonographic evaluation will take place just before and 30 minutes after stellate ganglion block. | No |
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