Propofol vs Propofol + Benzo/Opiates in High Risk Group
Status:
Terminated
Trial end date:
2014-07-01
Target enrollment:
Participant gender:
Summary
This will be a randomized controlled trial that compares the rates of sedation related
complications in high risk patients (ASA greater or equal to 3, BMI greater or equal to 30,
those at risk for OSA) undergoing advanced endoscopy procedures with propofol alone compared
to propofol in combination with benzodiazepines and opioids.