A observational study to assess the effectiveness of sphenopalatine ganglion block and tb caffiene in treatment of Post dural pucture headache FOLLOWING lower segment ceaserean sectio
Phase 4
- Conditions
- Health Condition 1: O00-O9A- Pregnancy, childbirth and the puerperium
- Registration Number
- CTRI/2022/10/046747
- Lead Sponsor
- Gajra raja medical college
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients who will give consent to participate in study
patients aged between 18 yaear to 50 year female
ASA physical grade 1 and 2
Exclusion Criteria
Patients refusal
uncoperative patients
history of facial trauma
coagulopathy or bleeding diathesis
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To evaluate the efficacy of sphenopalatine ganglion block in management of PDPH <br/ ><br>Timepoint: 24 week <br/ ><br>
- Secondary Outcome Measures
Name Time Method To asess the side effect of sphenopalatine ganglion blockTimepoint: To assess the side effect of tablet caffeine;TO assess the efficacy of oral caffeine 300 mg in management of PDPH.Timepoint: 24 week