To study pain relief after caesarean section by ultrasound guided erector spinae plane block.
Phase 4
- Conditions
- Health Condition 1: O94- Sequelae of complication of pregnancy, childbirth, and the puerperium
- Registration Number
- CTRI/2021/05/033746
- Lead Sponsor
- Government Medical College Baroda
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1) singleton, full term pregnancy
2) ASA Physical status â?? I or II
3) scheduled for elective LSCS under spinal anesthesia
Exclusion Criteria
1) Patients refusal and not able to understand study protocol.
2) Contraindication to spinal anesthesia.
3) Severe PIH
4) Patients with compromised renal and liver function, uncontrolled diabetes severe cardiovascular and respiratory disease.
5) Patients have allergy to any study drugs
Infection, trauma, scar or sinuses at site of block
6) BMI > 35 Kg/m2
7) If patient is taken under general anaesthesia at any point of time during the course of surgery.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare the duration of analgesia between control nd study groupTimepoint: Visual analogue scale score will be assessed after 2 hours of Erector spinae plane block
- Secondary Outcome Measures
Name Time Method 1)To compare the total amount of rescue analgesia required in first 24 h post <br/ ><br> Operatively. <br/ ><br>2. VAS scores at 2,4,6,8,12,18,24 hours. <br/ ><br>3. Hemodynamic parameter in both groups. [PR, BP, SPO2] post block <br/ ><br> <br/ ><br>4)complications of the technique and drugTimepoint: Baseline <br/ ><br>During procedure <br/ ><br>At 15,30,45, and 60minute. <br/ ><br>At 2,4,6,8,12,18,24hour