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Comparing effects of intravenous and nebulized magnesium sulphate for attenuation of laryngoscopic response

Comparison of Intravenous versus Nebulized Magnesium Sulphate on attenuation of hemodynamic response during laryngoscopy in patient undergoing elective surgery: a prospective, randomized, double blinded study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/02/040690
Enrollment
66
Registered
2022-02-28
Start date
Unknown
Completion date
Unknown
Last updated
2022-04-04

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

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: Group M NE: patient will recieve Magnesium Sulphate nebulisation (30mg/kg) diluted to 5ml nebulised over 15 minutes and Normal saline 50ml via infusion pump over 15 minutes Control Inte

Sponsors

none
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: American Society of Anaesthesiologists Physical status (ASA) I-II Patients undergoing elective surgery under general anaesthesia requiring endotracheal intubation

Exclusion criteria

Exclusion criteria: Anticipated Difficult laryngoscopy and intubation or more than one attempt for intubation taken. Patient having cardiovascular dysfunction. Uncontrolled Hypertensive Patients with raised intracranial pressure or intraocular pressure Pre-existing hepatic or renal impairment. Pregnant patients. Allergic to Study Drug. Patient refusal for consent.

Design outcomes

Primary

MeasureTime frame
changes in Mean Arterial Pressure and Heart Rate following intubationTimepoint: at the time of laryngoscopy, just after intubation, 1 min, 5 min and 10 min after intubation.

Secondary

MeasureTime frame
time taken to achieve TOF ratio of zeroTimepoint: during Induction;To compare propofol consumption during induction of anaesthesiaTimepoint: during induction;to look for incidence of bradycardia or hypotensionTimepoint: intraoperatively;to look for incidence of nausea or vomiting and respiratory depressionTimepoint: post operatively

Countries

India

Contacts

Public ContactDr Priyanka Gupta

all india institute of medical sciences, rishikesh

priyanka.anaes@aiimsrishikesh.edu.in9811894899

Outcome results

None listed

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