Feasibility of a New Ambulatory Multi-vital Signs Monitor
Stopped early · Not applicable
Conditions studied: Perioperative/Postoperative Complications
In brief
The purpose of this research is evaluate vital signs (VS), which include non-invasive blood pressure, pulse rate, respiratory rate and Oxygen Saturation (SpO2) using a portable wrist monitoring device called a Caretaker. This device has been cleared by the Food and Drug Administration (FDA) for use and allows the study team to check vital signs in a participant's normal setting. Participation in this study will involve wearing this portable device at 2 different time points: 1. for up to 24 hours immediately during and after the participant's preoperative visit to obtain baseline vital signs during normal activity and during sleep and 2. after surgery up to 24 hours while participant recovers prior to discharge from the hospital
Key facts
- Study ID
- NCT05562011
- Run by
- Wake Forest University Health Sciences
- People needed
- 61
- Starts
- 2021-08-18
- Expected to finish
- 2022-10-24
- Last updated by the study team
- 2023-12-20
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
Where it is running
- Wake Forest Health Sciences — Winston-Salem, North Carolina, United States
Full record on ClinicalTrials.gov
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