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Clinical Trials/PACTR202211634990263
PACTR202211634990263
Completed
未知

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

Dr Naa Martekuor Vanderpuye0 sites96 target enrollmentNovember 18, 2022

Overview

Phase
未知
Intervention
Not specified
Conditions
Surgery
Sponsor
Dr Naa Martekuor Vanderpuye
Enrollment
96
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
November 18, 2022
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
Dr Naa Martekuor Vanderpuye

Eligibility 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

  • Patients \< 18years because they are incapable of giving informed consent by law.
  • 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.

Outcomes

Primary Outcomes

Not specified

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