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Comparison of the effect of intravenous and intra-cuff magnesium on post-extubation tracheal morbidity.

Comparison of the effect of intravenous and intra-cuff magnesium on post-extubation tracheal morbidity.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
PACTR
Registry ID
PACTR202211634990263
Enrollment
96
Registered
2022-11-24
Start date
2022-04-01
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Surgery Anaesthesia

Interventions

Group A
Group B
Group C

Sponsors

Dr Naa Martekuor Vanderpuye
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Patients above 18 years requiring endotracheal intubation 2. Patients with BMI <30 3. Patients with ASA classification I or II All elective general surgery patients requiring endotracheal intubation who meet above inclusion criteria and give a signed or thumb-printed informed consent to participate in this study will be included except:

Exclusion criteria

Exclusion criteria: • Patients 18years of age who are mentally incapacitated. • Patients with ASA III and IV, as these may be too sick with uncontrolled co-morbidities. • Patients who have an Upper Respiratory Tract Infection prior to surgery (sore throat, cough, running nose), as these may make assessment of tracheal morbidities difficult. • Patients coming for head and neck surgeries as manipulations during these surgeries could in themselves cause laryngeal morbidity. • Patients who will have their surgical cases done in the prone position. • Patients with a history of Asthma. These patients have a reactive airway and are prone to airway complications during intubation. • Patients with a history of difficult intubations, anticipated difficult intubation, and those who will have multiple attempts at intubation. • Patients with known anatomical laryngo-tracheal abnormalities, snoring and gastroesophageal reflux. • Patients who will require post-operative intubation and so cannot have the occurrence of tracheal morbidity 24 hours post-operatively assessed. • Patients who are obese (BMI >35kg/m2) ( they are high risk for difficult intubation and ventilation as well as develop airway complications more easily)

Design outcomes

Primary

MeasureTime frame
It is expected that the subjects in the groups who had their ETT cuffs inflated with Magnesium Sulphate, or received intravenous Magnesium Sulphate, will have a reduction in the occurrence of post extubation sore throat, cough and hoarseness.

Secondary

MeasureTime frame
Heart rate and Blood pressures will be better controlled in the groups where the patients were given intravenous magnesium or intracuff magnesium

Countries

Ghana

Contacts

Public ContactEbenezer Owusu Darkwa

Supervisor

eoddarquah@yahoo.com+233244670149

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Aug 9, 2026