The usefulness of sphenopalatine ganglion block for postdural puncture headache
Not Applicable
- Conditions
- patients scheduled for epudural analgesia
- Registration Number
- JPRN-UMIN000035981
- Lead Sponsor
- Sapporo Medical University School of Medicine
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 30
Inclusion Criteria
Not provided
Exclusion Criteria
The sxclusion criteria were as follows: age younger than 20 years, allergy to local anesthetics, hemmorrhagic, and a surgical hinstory of the nasal cabvity.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Headache severity (Numerical rating scale) is ecaluated proior to sphenopalatine ganglion block, 1 hour, 24 hours, and 48 hours after the block.
- Secondary Outcome Measures
Name Time Method