The minimum effect-site concentration of propofol that is able to prevent the responses to stimuli used to evoke cranial reflexes - ND
- Conditions
- patients undergoing general anaesthesia for elective surgery
- Registration Number
- EUCTR2008-001037-98-IT
- Lead Sponsor
- POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Recruiting
- Sex
- All
- Target Recruitment
- Not specified
Inclusion Criteria
- age 18 years and older
- general anaesthesia for elective surgery
- ASA (American Society of Anaesthesiologists) I-II,
- BMI (Body Mass Index)< 30 Kg/m2,
- absence of airway difficulties (Mallampati III-IV) or analgesic therapy,
- lack of counter-indication to propofol usage
Are the trial subjects under 18? no
Number of subjects for this age range:
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range
F.1.3 Elderly (>=65 years) yes
F.1.3.1 Number of subjects for this age range
Exclusion Criteria
- maxillo-facial surgery
Study & Design
- Study Type
- Interventional clinical trial of medicinal product
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method