PACTR201607001643276

Propofol for laryngospasm

Low dose propofol versus lidocaine for relief of resistant post-extubation laryngospasm in the obstetric patient
Department of Anesthesia, Cairo University.·Not Applicable·Pan Africa Clinical Trials Registry·drugCompleted
Study focus
Disease/Condition
Respiratory; Other
Intervention type
drug
Sponsor & location
Primary sponsor
Department of Anesthesia, Cairo University.
Location
Egypt
Timeline & enrollment
Phase
Not Applicable
Start date
Jan 10, 2014
End date
Dec 20, 2015
Summary

Post-extubation laryngospasm is a life-threatening anesthetic emergency that needs prompt treatment. It is a dangerous complication that may lead to hypoxia or negative pressure pulmonary edema. Some studies listed laryngospasm as an anesthetic cause of obstetric mortality. Standard measures described for management of laryngospasm started with removal of the offending stimulus, jaw thrust, and positive airway pressure ventilation with 100% oxygen by bag and mask. When these measures fail, a small dose (0.1 mg/kg) of iv succinylcholine is used. Some studies suggested the use of topical or iv lidocaine. The use of small dose of propofol have been suggested for treatment of resistant laryngospasm in pediatric patients, because of its depressive effect on laryngeal reflexes. Other studies tried a small dose of propofol (0.5 mg/kg) for resistant laryngospasm in obstetric anesthesia.This work aims to compare the effectiveness of a small dose of propofol (0.5 ml/kg) versus lidocaine (1.5 mg/kg) for treatment of resistant post-extubation laryngospasm in obstetric patients, after failure of the standard measures and before the use of muscle relaxants.

ICD-10 classifications
Other specified respiratory disordersOther respiratory disordersOther diseases of the respiratory systemOther postprocedural respiratory disordersOther respiratory conditions due to chemicals, gases, fumes and vapours
Data source
Registry
Pan Africa Clinical Trials Registry
Trial ID
PACTR201607001643276
Type
Non-Device Trial
About this record

Access comprehensive clinical trial information for PACTR201607001643276 through Pure Global AI's free database. This Not Applicable trial is sponsored by Department of Anesthesia, Cairo University. and is currently Completed. The study focuses on Respiratory; Other.

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