Determining if the Buzzy® Personal Pain Relief Device Reduces Injection Pain of Propofol as Much as Intravenous Lidocaine in Children
Clinical trial NCT07770581 · TERMINATED
Trial details
- NCT number
- NCT07770581
- Sponsor
- Ann & Robert H Lurie Children's Hospital of Chicago
- Status
- TERMINATED
- Phase
- Not Applicable
- Study type
- INTERVENTIONAL
- Start date
- 2014-06-01
- Primary completion
- 2017-06-30
- Enrollment
- 49
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