Comparison of maternal hemodynamic parameters with the time taken and level of sensory and motor blockade
Not Applicable
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2024/03/063521
- Lead Sponsor
- Dr Jumana Afrin
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1. Parturients willing to give informed and written consent.
2. Singleton pregnant mothers
schedules for elective LSCS done under Sub Arachnoid block.
3. Parturients belonging to ASA ll
4. Height of parturients to be 150 to 170 cms.
Exclusion Criteria
1. Parturient refusal.
2. ASA lll and above
3. Parturients hypersensitive to study drug.
4. Parturients with significant coagulopathies and other contra
indications for spinal anaesthesia.
5. Parturients with pregnancy induced Hypertension.
6. Parturients with history of significant systemic disorders
(cardiovascular, respiratory or central nervous system)
7. Parturients with fetal anomalies and twin gestation.
8. Parturients with oligohydraminios.
9. Precious pregnancy.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method -Maternal heart rate, blood pressure, mean arterial pressure, oxygen <br/ ><br> <br/ ><br>saturation <br/ ><br>- level of sensory and motor blockade achieved <br/ ><br>time taken to attain maximum blockade <br/ ><br>- maximum blockade achievedTimepoint: Assessed preoperatively, at 2 minutes interval for first 10 minutes after <br/ ><br>sub arachnoid block, every 5 minutes for the next 20 minutes and every <br/ ><br>10 minutes thereafter for one hour.
- Secondary Outcome Measures
Name Time Method Intra & post operative adverse effects like itching, nausea, vomitingTimepoint: During procedure, <br/ ><br>1 hour after procedure