Adjusting local anaesthetic levels in spinal anaesthesia for safer and more comfortable ceasarean section- A study
Not Applicable
- Conditions
- Health Condition 1: O746- Other complications of spinal andepidural anesthesia during labor and delivery
- Registration Number
- CTRI/2024/08/072089
- Lead Sponsor
- Mahatma Gandhi Medical College
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.Term pregnancy (37 weeks)
2.Category IV - Planned for elective LSCS
3.Category III - Needing early delivery but no fetal or maternal compromise
4.Height more than 150 cms
5.ASA II
6.Singleton pregnancy
Exclusion Criteria
1.Hypertensive disorder complicating pregnancy
2.Cardiovascular illness
3.Fetal abnormalities
4.Height more than 180 cms
5.BMI more than 35
6.Other contraindications for spinal anaesthesia
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To estimate the incidence of hypotension following subarachnoid block with three different doses of bupivacaine at three different levels.Timepoint: At 1,2,4,6,8,10,12,15,20,25,30,35,40,60,90 minutes following subarachnoid block
- Secondary Outcome Measures
Name Time Method To estimate the spinal level achieved, time to achieve the level, total vasopressor required.Timepoint: At 1,2,4,6,8,10,12,15,20,25,30,35,40,60,90 minutes following subarachnoid block