Comparison of 0.75% Ropivacaine heavy and 0.5% Bupivacaine heavy in spinal anaesthesia for caesarean delivery
Phase 4
- Conditions
- Health Condition 1: O80- Encounter for full-term uncomplicated delivery
- Registration Number
- CTRI/2022/08/044691
- Lead Sponsor
- Mytily
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Obstetric patients coming for elective caesarean section
Age group of 20-40 years
ASA 1 & ASA 2 patients
Full term pregnant patients
Patients with Single live intrauterine fetus
Exclusion Criteria
1.Patients who refuse
2.Emergency surgeries
3.Age group <20 or >40 years of age
4.ASA 3 & ASA 4 patients
5.Pre term patients
6.Multiple pregnancy (twin or more gestation)
7.Associated comorbid conditions( PIH, GDM, Anaemia, Heart disease)
8.Bleeding diathesis patients
9.Fetal indication for caesarean delivery
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare the onset of sensory and motor block, duration of block with 0.75% ropivacaine and 0.5% bupivacaine in spinal anaesthesia for caesarean section.Timepoint: Every 5 minutes for 30 minutes and next 2 hours for regression
- Secondary Outcome Measures
Name Time Method To estimate the differences in hemodynamic variables ( BP, HR) and time for regression of sensory and motor block (assessed by modified Bromage scale) among both the groups.Timepoint: 2hours