A randomized control study to assess the efficacy of sphenopalatine ganglion block in patients with postdural puncture headache
Phase 4
- Conditions
- Anaesthesia
- Registration Number
- PACTR202401546543440
- Lead Sponsor
- Benha faculty of medicine
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- Female
- Target Recruitment
- 60
Inclusion Criteria
patients suffering from postdural puncture headache after spinal anesthesia not responding to usual reatment
Exclusion Criteria
patients with coagulopathy.,nasal septum deviation ,polyp, history of nasal bleeding and allergy to local anesthetics
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method