Central Line Clinical Trial
Official title:
Exploration of Central Venous Catheter Protective Devices in the Pediatric Population: A Mixed Methods Study
1. to determine the feasibility of utilizing a wearable device 2. to prospectively measure and evaluate parent and nurse satisfaction with the protective wearable device. This is a sequential, convergent mixed methods study design in which qualitative interview data will be collected first followed by quantitative data. Scheme and Outcomes: Identify eligible patients--Informed Consent--Provide education and two protective wearable device--Demographic data (electronic health record)--Interview parent on device--Every month complete 30-day satisfaction survey for a total of three data collection period-Discharge from study. Nurse data collection scheme: Study participants hospitalized at time of enrollment in study or anytime during the study period. Nurse of patients using device will complete satisfaction survey. Note: Vest is a Class I Exempt FDA-registered device.
n/a
| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Completed |
NCT04211116 -
Central Venous Catheters in Pediatric Anesthesia and Intensive Care
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| Completed |
NCT02314520 -
Complications Associated With Central Venous Access in the NSICU: PICC vs CVC
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N/A |