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Clinical Trial Summary

This study will examine the use of the ivWatch Model 400 to monitor PIV sites in pediatric patients. Half the participants will be monitored by the device without infiltration notifications and the other half will be monitored by the device with infiltration notifications enabled.


Clinical Trial Description

n/a


Study Design

Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Diagnostic


Related Conditions & MeSH terms

  • Infiltration of Peripheral IV Therapy

NCT number NCT02553421
Study type Interventional
Source ivWatch, LLC
Contact
Status Completed
Phase N/A
Start date August 2015
Completion date July 2016

See also
  Status Clinical Trial Phase
Completed NCT02120443 - ivWatch Model 400: Device Validation for Non-Infiltrated Tissues N/A
Completed NCT02123745 - ivWatch Model 400: Device Validation for Infiltrated Tissues N/A
Completed NCT04064229 - ivWatch Sensor: Device Validation for Infiltrated Tissues N/A
Completed NCT04065373 - ivWatch SmartTouch Sensor: Device Validation for Non-Infiltrated Tissues N/A