The purpose of this study is to explore how the timing of procedural sedation medications influences patient comfort and satisfaction with sedation. Participation in this study will included be randomly assigned to one of two groups (long and short) within standard of care. Each group will observe a time interval between receiving procedural sedation medications and the start of the procedure. A trained observer will evaluate patient experience during the procedure and at the end of the procedure we will ask the participant 3 brief questions about the experience. All other information collected about the experience during the procedure will occur as part of usual care. No further activities will be asked as part of this study. All study activities will occur during a scheduled visit and participation is complete once questions have been answered.
Study Type
OBSERVATIONAL
Enrollment
175
Duke University
Durham, North Carolina, United States
Total medication administration dosage as measured by the procedural database
Time frame: During procedure, up to 2.5 hours
Frequency of medication administration as measured by the procedural database
Time frame: During procedure, up to 2.5 hours
Patient satisfaction as measured by Procedural Sedation Assessment Survey (PROSAS)
Time frame: Within 2 hours of procedure
Pain as measured by observation using the Behavioral Pain Assessment Tool (BPAT)
Time frame: During procedure, to 2.5 hours
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.