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Magnesium sulphate and its help in reducing the postoperative pain and ileus

A RANDOMISED CONTROLLED TRIAL TO STUDY THE EFFECT OF PREOPERATIVE SYSTEMIC MAGNESIUMSULFATE INFUSION ON POST OPERATIVE PAIN AND POST OPERATIVE ILEUS FOLLOWING NON LAPAROSCOPIC MAJOR ABDOMINAL SURGERIES - NIL

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/09/094904
Enrollment
100
Registered
2025-09-16
Start date
Unknown
Completion date
Unknown
Last updated
2025-10-13

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

Conditions

Health Condition 1: 4- Measurement and Monitoring

Interventions

Intervention1: MagnesiumSulphate: 40mg/kg magnesium sulfate in 100ml ns 30 minutes before induction as IV infusion Control Intervention1: normal saline: normal saline infusion given preoperatively

Sponsors

Chettinad Hospital and Research Institute
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients of age more than 18 and less than 60 years. Patients undergoing open abdominal surgeries. Patients who received ASA 1, 2 in Pre anaesthetic check. Patients with normal Serum Magnesium levels. Patients who consented to be included in the study

Exclusion criteria

Exclusion criteria: Patients of age less than 18 and more than 60 years. Patients with Liver failure, Renal failure, Heart block, Arrythmia, EF less than 45 percent, Pregnancy, Neurological disorders, Hypersensitivity Patients with serum magnesium above normal. Patients with Blood glucose more than 200mg/dl on the day of surgery. Patient on Calcium channel blockers. Patients undergoing laparoscopic abdominal surgeries Those who don not give consent to be included in the study.

Design outcomes

Primary

MeasureTime frame
to assess the reduction of duration of post operative ileus on Mgso4 infusionTimepoint: 1, 2, 4, 12, 24 hrs post operatively

Secondary

MeasureTime frame
to assess the reduction of post operative pain on Mgso4 infusionTimepoint: 1, 2, 4, 12, 24 hours post operatively

Countries

India

Contacts

Public ContactDr K Muthu Raj

Chettinad hospital and research institute

drmuthurajkasinathan@gmail.com7305705536

Outcome results

None listed

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