Propofol for laryngospasm
Not Applicable
Completed
- Conditions
- RespiratoryLaryngospasm
- Registration Number
- PACTR201607001643276
- Lead Sponsor
- Department of Anesthesia, Cairo University.
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 78
Inclusion Criteria
All parturients of ASA class I or II, who were scheduled for cesarean section under general anesthesia, suffered from post-extubation laryngospasm.
Exclusion Criteria
known sensitivity to lidocaine or propofol
upper respiratory tract infection
history of bronchial asthma or other lung diseases
chronic smoking
chronic exposure to smokers, dust or fumes.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method