MedPath

Evaluation of effect of addition of magnesium sulphate to bupivacaine for spinal anaesthesia in pregnant women

Completed
Conditions
ASA I/II parturients
Registration Number
CTRI/2015/05/005749
Lead Sponsor
Lady Hardinge Medical College
Brief Summary

The aim of our study was to evaluate whether addition of magnesium sulphate to intrathecal hyperbaric bupivacaine has any effect on prolonging the duration of postoperative analgesia as compared to hyperbaric bupivacaine alone, in patients undergoing lower segment Caesarean section. Also to compare the onset & duration of sensory and motor blockade, neonatal outcome and side-effects, in the two groups. 

We found that magnesium sulphate (50mg) as an adjuvant to hyperbaric bupivacaine intrathecally produces a significant prolongation in the duration of postoperative analgesia in patients undergoing lower segment Caesarean section.. It produces a sensory block of significantlylonger duration as compared to hyperbaric 0.5% bupivacaine alone ; but a prolongation in the duration of motor block whichis seen with magnesium sulphate is not desirable as it delays the earlymobilisation of patients.  However,magnesium sulphate as an adjuvant to bupivacaine maybe beneficial in stableeclamptic patients or patients in whom side-effects related to intrathecalopioids aren’t desirable in prolonging the duration of post-operativeanalgesia. The incidence of hypotension andbradycardia were also comparable between the two groups.

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Female
Target Recruitment
100
Inclusion Criteria

ASA I and II parturients Undergoing lower segment Caesarean section.

Exclusion Criteria

patient refusal any contraindication to regional anaesthesia weight>90kg height<145 or >170cm known allergy to local anaesthetic or magnesium sulphate dysrrthymias in ECG or any systemic disorder history of chronic pain already on magnesium therapy severe psychiatric disturbance history of drug abuse unable to communicate in either hindi or english.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Prolongation in duration of postoperative analgesia with addition of intrathecal magnesium sulphate to hyperbaric bupivacaine as compared to hyperbaric bupivacaine with normal salinetime interval between administration of intrathecal block and first request for analgesia by patient(visual analog score more than 4 ) was noted
Secondary Outcome Measures
NameTimeMethod
Onset of sensory & motor block was slower while duration of sensory as well as motor block was prolonged with magnesium sulphate group. Neonatal APGAR scores and incidence of side-effects were comparable in the two groupsContinuous ECG,HR,SpO2 were monitored. Non-invasive BP,PR & level of sedation at every 3min interval till delivery of baby,thereafter at 5min interval till end of surgey,postop at 30min interval for first 2hr then hourly till first recue analgesic

Trial Locations

Locations (1)

lady hardinge medical college, new delhi

🇮🇳

Delhi, DELHI, India

lady hardinge medical college, new delhi
🇮🇳Delhi, DELHI, India
SUSHMITA ROY
Principal investigator
7838553257
mita.sush17@gmail.com

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.