A randomized prospective comparative study of incidence of post dural pucture backache(PDPB) following median and paramedian approach for administration of subarachnoid block in patients undergoing cesarian sectio
Phase 1
- Conditions
- Health Condition 1: O745- Spinal and epidural anesthesia-induced headache during labor and delivery
- Registration Number
- CTRI/2024/05/066701
- Lead Sponsor
- Tata Main Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patient undergoing elective / emergency cesarean section
ASA grades |-|||
Exclusion Criteria
Patients refusing to participate in the study
History of allergy to local anesthetics
Patients with coagulopathy or infection at the site of block
Patients with psychiatric illness or cognitive dysfunction
Patients with the history of previous back surgery, spondylolisthesis, and other lumbar disorders
Previous history of low back pain
Failure of spinal anesthesia
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To determine the incidence of post-dural puncture backache (PDPB) in both groups in the first 3 months postoperativelyTimepoint: 3 months postoperatively
- Secondary Outcome Measures
Name Time Method Backache on Numerical Rating Scale (NRS) in both groups after 24 hours,1 week, 1 month, 2 months and 3 months postoperatively <br/ ><br>The number of attempts required at subarachnoid block by either approach <br/ ><br>Total requirement of additional analgesics for low backache in first 24 and 48 hours postoperatively (Morphine equivalents) <br/ ><br>Compare the incidence of PDPH in the two groups in first 72 hours <br/ ><br>Timepoint: 24 and 48 hours, 72 hours