Skip to main content
Clinical Trials/CTRI/2025/01/079710
CTRI/2025/01/079710Not yet recruitingPhase 2

A comparative study of intravenous magnesium sulphate and nebulization of magnesium sulphate on attenuation of intubation response and airway pressure in patients undergoing laparoscopic surgeries, a randomized control trial.

Bangalore Medical College and Research Institute1 site in 1 country96 target enrollmentStarted: February 10, 2025Last updated:

Trial Snapshot

Phase
Phase 2
Status
Not yet recruiting
Sponsor
Enrollment
96
Locations
1
Primary Endpoint
To compare hemodynamic response after intubation.

Study Overview

Brief Summary

Endotracheal intubation is an important component of general anesthesia. Laryngoscopy causes stimulation of sympathetic nervous system and causes increase in concentration of catecholamines like adrenaline and noradrenaline. This can cause left ventricular failure, renal failure, surgical bleeding, cerebral hemorrhage and myocardial ischemia in patients with general anesthesia. Various drugs like Magnesium sulphate , lidocaine, dexmedetomidine can be used in attenuating response to intubation.

The current Randomized controlled trial is carried out to compare attenuation response of magnesium sulphate in two different route of administration  i.e, intravenous and nebulization as studies comparing them are scarce.

Study Design

Study Type
Interventional
Allocation
Randomized
Masking
Participant, Investigator and Outcome Assessor Blinded

Eligibility Criteria

Ages
18.00 Year(s) to 60.00 Year(s) (—)
Sex
All

Inclusion Criteria

  • Patients aged between 18 to 60 years .
  • Patients willing to give informed written consent Patients with ASA Grade 1 and Grade 2 Patients scheduled for surgeries under general anaesthesia for laparoscopy.

Exclusion Criteria

  • Patients refusal to give informed written consent Patients belonging to ASA Grade 3, 4, 5 Patients with cardiovascular, respiratory, renal and hepatic derangement Patients with history of drug allergy Pregnant women Patients with anticipated difficult airway.

Outcomes

Primary Outcomes

To compare hemodynamic response after intubation.

Time Frame: AT Basal, 2min, 5 min and 7 min after intubation

Secondary Outcomes

  • To compare peak airway pressures after intubation.(At Basal , 2 min , 5 min, 7 min after intubation)

Investigators

Sponsor
Bangalore Medical College and Research Institute
Sponsor Class
Government medical college
Responsible Party
Principal Investigator
Principal Investigator

Dr Sathya H

Bangalore Medical College and Research institute, Bangalore

Study Sites (1)

Loading locations...

Similar Trials