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Effect of intravenous magnesium sulphate to attenuate the hemodynamic stress response of pneumoperitoneum in patients undergoing laparoscopic cholecystectomy.

Effect of intravenous magnesium sulphate to attenuate the hemodynamic response to carbon dioxide pneumoperitoneum in patients undergoing laparoscopic cholecystectomy: a randomized controlled study - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/09/073343
Enrollment
64
Registered
2024-09-04
Start date
Unknown
Completion date
Unknown
Last updated
2024-09-16

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

Conditions

Health Condition 1: K802- Calculus of gallbladder without cholecystitis

Interventions

Intervention1: Inj. Magnesium Sulphate (50% w/v) 30mg/kg diluted in 20ml of 0.9% normal saline.: Study participants will be randomized into two groups. Intervention group will receive Inj. Magnesium s

Sponsors

Rohan Deb
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients of American Society of Anesthesiologists (ASA) grade I or II 2. Patients of age group 20-60 years.

Exclusion criteria

Exclusion criteria: 1. Patients with anticipated difficult intubation 2. Patients with hypermagnesemia 3. Patients with history of allergy to magnesium sulphate 4. Patients with severe hepatic, renal, endocrine dysfunction 5. Patients with cardiovascular disorder 6. Conversion to open procedure

Design outcomes

Primary

MeasureTime frame
Attenuation of hemodynamic changes to pneumoperitoneum such as systolic blood pressure (SBP), diastolic blood pressure (DBP), mean arterial pressure (MAP) and heart rate (HR)Timepoint: Outcome will be assessed starting from the point of administration of study drugs till 60 minutes post pneumoperitoneum. Data will then be assessed at the end of one year.

Secondary

MeasureTime frame
Documentation of side effects such as bradycardia, hypotension, if encounteredTimepoint: Outcome will be assessed starting from the point of administration of study drugs till 30 minutes post extubation. Data will then be assessed at the end of one year.

Countries

India

Contacts

Public ContactLongjam Eshori

Regional Institute of Medical Sciences, Imphal

drlongjam@gmail.com9436036407

Outcome results

None listed

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