N/A
N=100
Vibration Analgesia in Propofol Infusion During Anesthesia Induction
Pain, Acute
Bottom Line
View on ClinicalTrials.gov: NCT03509857 ↗Enrolled (actual)
100
Serious AEs
0.0%
Results posted
Sep 2022
Primary outcome: Primary: Level of Pain as Observed by Two Independent Observers Following Propofol Injection, With or Without a Vibration Analgesia Adjunct — 3.1; 1.4 units on a scale
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- BUZZY(tm) (Device); No Intervention (Other)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- Montefiore Medical Center
- Primary completion
- Nov 2019
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Level of Pain as Observed by Two Independent Observers Following Propofol Injection, With or Without a Vibration Analgesia Adjunct |
3.1; 1.4 | — |
Summary
In this study, the investigators seek to evaluate the role of vibration in the reduction of discomfort associated with painful stimulus associated with anesthesia induction. Through this study, the investigators hope to develop a comprehensive and cost-effective approach to minimize patient discomfort during anesthesia induction.
Eligibility Criteria
Inclusion Criteria
- Those aged 18 to 100 who are going to receive propofol injection as part of induction of anesthesia for surgery
Exclusion Criteria
- Those below the age of 18
Data sourced from ClinicalTrials.gov (NCT03509857). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.