Race-Specific Propofol Titration to Effect for Procedural Sedation

Completed

Conditions studied: Unconsciousness, Apnea, Postanesthetic, Sedative Overdose, Hypoxemia

In brief

Prospectively evaluate newly established guidelines and make clinicians aware of inter-racial difference in propofol sensitivity.

Key facts

Study ID

NCT03290859

Run by

University of Florida

People needed

2780

Starts

2018-01-05

Expected to finish

2019-02-05

Last updated by the study team

2019-10-25

Who can join

Age: 18 and older, up to 80. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Patients undergoing propofol sedation at Gainesville (GNV) and Jacksonville (JAX) GI Endoscopy suites
• Age range 18 - 80 years old
• Patients whose race can be identified from the electronic patient information chart (EPIC)

You may not qualify if…

• Patients who identify as multiracial in Epic
• Patients who identify as Other in Epic
• Patients who refuse to indicate their race in Epic
• Patients whose race is listed as unknown in Epic

Where it is running

• UF Health — Gainesville, Florida, United States

Full record on ClinicalTrials.gov

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