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Study identifier: NCT07328893 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Effect of Single Dose Intravenous Magnesium Sulfate on Postoperative Analgesic Consumption in Patients Undergoing Laparoscopic Cholecystectomy

Condition: Analgesia; Postoperative  ·  Sponsor: Tata Main Hospital

PhasePhase 4
Planned participants106
Who can joinAll sexes, 18 Years to 65 Years
Healthy volunteersNo

About this study

This study describes a randomized controlled trial designed to evaluate the impact of a single intravenous dose of magnesium sulfate on postoperative analgesic consumption in patients undergoing laparoscopic cholecystectomy. The primary aim is to determine if magnesium sulfate can reduce postoperative morphine usage and its associated side effects. The study will involve 106 patients (53 per arm), aged 18-65, classified as ASA physical status I or II, who are scheduled for elective laparoscopic cholecystectomy. Participants will be randomly assigned to receive either 30 mg/kg intravenous magnesium sulfate or a placebo (normal saline), alongside standard anesthetic care. Secondary outcomes include pain scores, the time until rescue analgesia is needed, and the monitoring of hemodynamic responses and potential adverse events. Statistical analysis will utilize descriptive statistics, chi-square tests, and t-tests or Mann-Whitney U-tests to compare the two groups.

This description comes directly from the study's public registry record.

Talk to the study team

Dr Deb Sanjay Nag, MD  ·  9431166582  ·  debsanjay@gmail.com

Himanshu Kumar, DNB  ·  7763807104  ·  himanshu.kumar@tatasteel.com

Always discuss trial participation with your own doctor first.

Locations (2)

Tata Main HospitalJamshedpur, Jharkhand, IndiaRecruiting
Dr.Deb Sanjay NagJamshedpur, Jharkhand, IndiaRecruiting

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Source record: clinicaltrials.gov/study/NCT07328893