Overview

Effect Site Controlled, Reaction Time Safeguarded, Patient Maintained Sedation With Propofol in Healthy Volunteers

Status:
Completed
Trial end date:
2006-09-01
Target enrollment:
0
Participant gender:
All
Summary
Whether patient-maintained sedation (the patient controls his/her degree of sedation using a hand-held device) using the drug propofol is safer and more effective when using deteriorating reaction time as an added safeguard against the small potential for over sedation in a group of healthy volunteers.
Phase:
Phase 4
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
Sonia Allam
Collaborator:
NHS Greater Glasgow and Clyde
Treatments:
Propofol
Criteria
Inclusion Criteria:

- ASA I or II (healthy or mild systemic illness) healthy volunteers

- Age 18 - 50

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 or breastfeeding

- Unable or unwilling to give informed consent

- Unable to use necessary apparatus

- Vulnerable groups