A clinical trial to study the effects of two drugs, Fentanyl and Butorphanol in combination with another drug Propofol for general anaesthesia using a device called Laryngeal mask airway.
Phase 3
Not yet recruiting
- Conditions
- Health Condition 1: null- Classical Laryngeal Mask Airway insertion condition on American Society of Anaesthesiologists Physical Status I and II patients who require requires general anaesthesia for short surgical procedures
- Registration Number
- CTRI/2013/08/003881
- Lead Sponsor
- I
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Not Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 40
Inclusion Criteria
Adult males or females of age group 18 to 55 years who comes under the American Society of Anaesthesiologists (ASA) Physical Status I and II for short surgical procedures who need LMA for maintaining general anaesthesia.
Exclusion Criteria
Patients of the American Society of Anaesthesiologists (ASA) Physical Status III and IV, those who suffer from pharyngeal pathology, low pulmonary compliance or history of allergy to Propofol, Butorphanol and Fentanyl.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Jaw relaxation according to Youngâ??s criteriaTimepoint: 60 seconds following the studied drug and Propofol is administered
- Secondary Outcome Measures
Name Time Method Overall LMA insertion condition according to modified Scheme of Lund and StovenerTimepoint: 60 seconds following the studied drug and Propofol is administered