Sphenopalatine Ganglion Block For Post-Dural Puncture Headache In Obstetric Parturients
Not Applicable
- Conditions
- Health Condition 1: O745- Spinal and epidural anesthesia-induced headache during labor and delivery
- Registration Number
- CTRI/2022/05/042612
- Lead Sponsor
- Sir Ganga Ram Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
All consenting obstetric parturients aged 18-45 years who receive neuraxial block for labour or caesarean delivery with development of PDPH within 72 h of dural puncture will be eligible to participate.
Exclusion Criteria
Parturient with chronic neurological disorder (epilepsy), bleeding disorder, allergy to local anaesthetics, deformity of the nasal septum, nasal polyps, frequent nosebleeds, those with nasal or sinus surgery within the past year or refusal to participate will be ineligible to participate
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To assess efficacy of SPG block in terms of pain relief after PDPHTimepoint: 5min, 30 min, 2h, 4h, 8h,12h, 24h and 48 h
- Secondary Outcome Measures
Name Time Method A.To observe at different time intervals <br/ ><br>1)Pain relief in supine and sitting position <br/ ><br>2)Numerical rating score (NRS) more than 3 in sitting position <br/ ><br>B.Time to first analgesic dose after the SPG block <br/ ><br>C.Relief in associated symptoms of PDPH (nausea, vomiting, visual changes, neck pain and stiffness) <br/ ><br>D.Presence of adverse effects (discomfort, change in taste, numbness in throat, epistaxis) associated with the block <br/ ><br>E.Need for epidural blood patch <br/ ><br>F.Parturient satisfaction <br/ ><br>Timepoint: 5min, 30 min, 2h, 4h, 8h,12h, 24h and 48 h