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To determine effect of intravenous magnesium sulphate on spinal anesthesia for Caesarean section in pre eclamptic patients.

Effect of intravenous magnesium sulphate on bupivacaine spinal anaesthesia for elective lower segment Caesarean section in pre eclamptic patients. A randomised, Double blind, controlled interventional study at S.M.S Medical college and hospital, Jaipur during 2020-2022

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/08/035418
Enrollment
84
Registered
2021-08-04
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: O149- Unspecified pre-eclampsia

Interventions

Intervention1: Injection magnesium sulphate: Intravenous magnesium sulphate 15min before giving hyperbaric bupivacaine .5% spinal anesthesia. Intervention2: Injection magnesium sulphate: Intravenous

Sponsors

Department Of Anesthesiology
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patients of preeclampsia undergoing elective caesarean section: 2.Systolic blood pressure 140-160mmHg 3.Diastolic blood pressure >90mm hg 4.Proteinuria 5.Body weight 45 to 70 kg 6.Height-145-165cm 7.Patients without headache, dizziness, and dyspnea

Exclusion criteria

Exclusion criteria: 1.Patients not willing to participate in the study. 2. Cases with sepsis, bacteremia or skin infection of local site 3. History of severe hypovolemia, anemia and compromised renal, cardiac or respiratory status 4. Cases with raised intracranial tension 5. History of blood coagulopathies â?? Patient allergic to drugs used for study

Design outcomes

Primary

MeasureTime frame
To determine the difference in characterstics of nerve block and duration of analgesia in both groups.Timepoint: Baseline to 24 hour postoperative.

Secondary

MeasureTime frame
1.To determine the difference in change in hemodynamic variables (Heart Rate; Mean Blood Pressure; Systolic Blood Pressure; Diastolic Blood Pressure). 2.To compare the proportion of cases with complications. Timepoint: Baseline to 24 hour postoperative

Countries

India

Contacts

Public ContactDr Prashant Santlani

S.M.S Medical College

Trishala.jain31@gmail.com

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026