A Pilot Trial of Continuous Portable Postoperative Hemodynamic And Saturation Monitoring On Hospital Wards
Completed · Not applicable
Conditions studied: Hemodynamic Instability, Respiratory Complications of Care
In brief
The study team will collect data for this study from participants who are having surgery and recovering postoperatively on 2 pre-designated hospital units. The study team will use vital signs data from a portable device that participants wear on their wrists as well as conventional vital signs data that is collected when a health care provider comes into their room and collect this information. A substudy is also being performed with the distribution of surveys to the nursing staff on the floors who are utilizing the ViSi hemodynamic monitors within our institution.
Key facts
- Study ID
- NCT04574908
- Run by
- Wake Forest University Health Sciences
- People needed
- 879
- Starts
- 2020-10-07
- Expected to finish
- 2021-10-08
- Last updated by the study team
- 2024-05-21
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- >/= 65 years of age
- >/= 45 years of age with at least 1 cardiovascular risk (hypertension, diabetes)
- Requiring a general or regional anesthetic as part of their surgical procedure.
- Requiring (or anticipated to require) at least a 48 hour hospital stay after surgery.
- All subjects aged 18 and older who are patients receiving ViSi monitoring on the 2 nursing units involved.
You may not qualify if…
- < 48 hour hospital stay
- Receiving local anesthetic for their surgical procedure
- troponins not ordered if <65 years of age without a single cardiovascular risk factor or <45 years of age
Where it is running
- Wake Forest Univesity Health Sciences — Winston-Salem, North Carolina, United States
Full record on ClinicalTrials.gov
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