Health Condition 1: O82- Encounter for cesarean delivery without indication
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Patient undergoing LSCS 2. Age 18-40 years 3. ASA II patients 4. Weight 50-80 kgs 5. Height 155cm-170cm 6. Singleton pregnancy
Exclusion criteria
Exclusion criteria: 1. Emergency caesarean section 2. Patients refusing spinal anesthesia 3. Infection at the site of regional blockade 4. Bleeding diathesis 5. Hypersensitivity to the study drug 6. Allergy to local anaesthetics 7. Neurological diseases 8. Spinal deformities
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To assess and compare the duration of sensory block in both groupsTimepoint: Every 15 mins after completion of surgery | — |
Secondary
| Measure | Time frame |
|---|---|
| To assess quality of block as assessed by patient and surgeonTimepoint: Once in postoperative period;To assess complicationsTimepoint: Every hourly during Intraoperative and postoperative period till 48 hours;To assess onset of sensory and motor blockTimepoint: Every 15 seconds after spinal;To assess total vasopressor and atropine usedTimepoint: Once in postoperative period;To compare APGAR scoreTimepoint: At 0, 1 and 5 min after delivery of baby;To compare duration of motor block between two groupsTimepoint: Every 15 mins after completion of surgery;To compare the hemodynamic profile (heart rate and blood pressure) between the two drugs.Timepoint: Baseline, pre spinal, post spinal, 5min,15 min,30 min,60 min,120 min, PACU | — |
Countries
India
Contacts
Saveetha Medical College and Hospital