ivWatch in Prevention of Extravasation of Vesicants in an Oncology Setting
Completed · Not applicable
Conditions studied: Oncology, Extravasation
In brief
This study aims to determine the feasibility of using the ivWatch (registered trademark) device to determine if there is an infiltration at the site of a peripheral intravenous (PIV) catheter. An infiltration is when the IV fluid leaks out of a vein and into the surrounding tissue. If medication starts leaking outside the vein, it can cause damage to the surrounding tissue. Using the ivWatch device may identify leaking fluid before the nurse is able to visually observe the signs or symptoms of the leaking fluid.
Key facts
- Study ID
- NCT06758011
- Run by
- Roswell Park Cancer Institute
- People needed
- 2400
- Starts
- 2023-05-17
- Expected to finish
- 2026-01-26
- Last updated by the study team
- 2026-02-17
Who can join
Age: 18 and older, up to 95. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Patients requiring a peripheral IV for infusion of vesicant or vesicant-like agents (chemotherapy, other vesicant medications).
- PIV must be inserted
- Participant (or legal representative) must understand the nature of this study and verbally consent with the Research Study Information Sheet prior to receiving any study related procedure
You may not qualify if…
- Patients who are not getting a vesicant, irritant or vesicant like fluid infused.
- Patients who are bruised, scarred, or tattooed in the area of the PIV.
- Patients with skin integrity issues at the site of the PIV.
- Patients who are on "light precautions."
- Not for use in power injectors.
- Not for use on mediports, implanted ports, IVAD, central lines, PICC lines.
- Patients without a cancer diagnosis.
Where it is running
- Roswell Park Comprehensive Cancer Center — Buffalo, New York, United States
Full record on ClinicalTrials.gov
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