Effect site controlled, reaction time safeguarded, patient maintained sedation with Propofol A)in oral surgery patientsB)in general dentistry patientsC)in colonoscopy patients - Patient maintained sedation with the added safeguard of reaction time.
- Conditions
- o specific medical condition. IMP will be used to provide conscious sedation for patients undergoing potentially unpleasant procedures including dentistry and colonoscopy.
- Registration Number
- EUCTR2005-005758-39-GB
- Lead Sponsor
- Greater Glasgow Health Board
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Recruiting
- Sex
- All
- Target Recruitment
- Not specified
Inclusion Criteria
ASA I or II (healthy or mild systemic illness) undergoing planned dental surgery or colonoscopy.
Age 18 - 65
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) no
F.1.3.1 Number of subjects for this age range
Exclusion Criteria
ASA III or above
Out with age group above
Contraindication to propofol
History of epilepsy
History of substance abuse
Major Psychiatric illness
Pregnancy
Unable or unwilling to give informed consent
Unable to use necessary apparatus
Vulnerable groups
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