Propofol vs Propofol + Benzo/Opiates in High Risk Group

Stopped early · Not applicable

Conditions studied: Sleep Apnea, Obstructive, Obesity

In brief

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.

Key facts

Study ID

NCT01315158

Run by

Washington University School of Medicine

People needed

36

Starts

2011-01-01

Expected to finish

2014-07-01

Last updated by the study team

2016-10-28

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Ability to provide informed consent
• Age greater than or equal to 18 years
• Presence of at least 1 of the following criteria:
• ASA class 3 or higher
• BMI of 30 or greater
• At risk for OSA (score of 3 or greater on the STOP-BANG screening tool)

You may not qualify if…

• drug allergy to Propofol, Benzodiazepines, or Opioids
• patients who received Benzodiazepines or Opioids within 24 hours of the procedure

Where it is running

• Washington University School of Medicine — St Louis, Missouri, United States

Full record on ClinicalTrials.gov

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