study comparing the efficacy of post operative pain control with use of injection in spinal fluid with pain control drug vs usg guided regional pain control injection near surgical site in muscles in LSCS patients operated under spinal anaesthesia
Phase 3
Completed
- Conditions
- Health Condition 1: O998- Other specified diseases and conditions complicating pregnancy, childbirth and the puerperium
- Registration Number
- CTRI/2024/01/061837
- Lead Sponsor
- Dr Apoorva
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Asa2 pregnant patients
Exclusion Criteria
Co morbid illnesses, contraindication spinal
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Post op analgesia using the VAS score for pain and if more than 4 rescue analgesics given IVTimepoint: Post op analgesia at 0,1,2,4,6,12,18,24 hours using VAS score
- Secondary Outcome Measures
Name Time Method Post operative nausea & vomiting, post operative sedation of patient APGAR score of newborn born out of LSCSTimepoint: Post operative nausea, vomiting & sedation noted at 0,1,2,6,12,18,24 hours. APGAR SCORE of baby at 0,1,3,5 minutes after birth.