Effect of hyperbaric Ropivacine in comparison to Bupivacaine for spinal anaesthesia

Phase 3

Recruiting

• Conditions: Delivery by elective Caesarian section.; Single delivery by elective caesarean section; O82.0

• Registration Number: IRCT20221109056455N1
• Lead Sponsor: Tata Main Hospital, Jamshedpur

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 21 August 2023

Recruitment & Eligibility

• Status: Recruiting
• Sex: Female
• Target Recruitment: 98

Inclusion Criteria

ASA physical status 1 and 2
Pregnant adults for elective caesarean section

Exclusion Criteria

Allergy to Ropivacaine or Bupivacaine
Infection at the site for spinal anaesthesia
Patient with evidence of foetal distress
Short stature (150 cm)
Tall stature (>180 cm)
Obesity(BMI>30)
Patient with an obstetrical complication (multiple gestations, bleeding, gestational hypertensive diseases)
Psychiatric or seizure disorder
Bleeding disorder
Cardiac disease

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Duration of motor blockade monitored by Bromage scale. Timepoint: 30 min. Method of measurement: Bromage score.

Secondary Outcome Measures

Name	Time	Method
Onset of sensory blockade. Timepoint: every 2 minutes after spinal block. Method of measurement: pin prick method.;Onset of motor blockade. Timepoint: every 2 minutes after spinal block. Method of measurement: Modified Bromage score.