Clinical Research Details

Descriptive Information
A comparison of sevoflurane-propofol versus sevoflurane or propofol for laryngeal mask airway insertion in adults

Sahar Sayyid
ss01@aub.edu.lb

15781547
Completed

Clinical Research - Clinical Trials (phase 0, 1,2 3 & 4)  


No
Collaborators
  • Marie Aouad Maroun
  • Samar Taha
  • Musa Mouallem
  • Anis Baraka
Coordinators
Fadia Shebbo
fs97@aub.edu.lb
Extension: 5411
Conditions and Keywords
laryngeal mask airway insertion in adults
laryngeal mask airway insertion;sevoflurane;propofol
Study Design
Eligibility and IRB
Both
Min:
Max:
Yes
No







adult ASA physical status I–II patients aged 18–65 yr undergoing elective orthopedic, plastic, or gynecologic procedures were enrolled in the study.

Day surgery cases and in-patients were included. Patients with a history of difficult intubation (or likely to be difficult to intubate), gastroesophageal reflux, allergy, or sensitivity to volatile anesthetics or to propofol, those with a body mass index more than 1.5 times normal, heavy smokers (>=20 cigarettes per day), and patients taking any sedative drugs that influence the induction anesthetic were excluded from the study