Williamsburg, Va. — ivWatch, LLC recently began assessing the efficacy of its inaugural medical device, the ivWatch Model 400, on pediatric patients at Cincinnati Children’s Hospital Medical Center. The medical device company works to improve patient safety in infusion therapy and vascular access.

The ivWatch Model 400 is used to assist medical professionals in detecting when intravenous (IV) fluids have leaked out of the vein and into the surrounding tissue, called a PIV infiltration. The device already has received FDA clearance for use on adults 18 and over.

The goal of the pediatric clinical trial is to measure the performance of the device for detecting infiltrated PIV sites of pediatric patients. The phase II pilot study began on Aug. 25, 2015 and is anticipated to last six to nine months.

PIV therapy is one of the most common invasive procedures performed in U.S. hospitals. Failures can occur when the infusate leaks into surrounding tissue. Pediatric patients may be at higher risk of infiltration due to their heightened activity levels, limited communication skills and small limb size.

“As one of the nation’s top pediatric hospitals, Cincinnati Children’s is committed to advancing patient safety,” said Darcy Doellman MSN, RN, CRNI, VA-BC, principal investigator, clinical manager of the Vascular Access Team, and an industry recognized vascular access expert. “The insights we gain by hosting the ivWatch pediatric trial should contribute to improved understanding of IV therapy monitoring practices for pediatric patients across the U.S.”

Co-investigators of the study include Sylvia Rineair, MSHA, BSN, RN, VA-BC, Candice Fletcher Overly, MSN, RN, NSQIP, SCR and Dr. Neil Johnson, an interventional radiologist.

Current nursing practice for monitoring pediatric patients with a PIV involves regular visual and tactile assessment of the PIV site. The ivWatch Model 400 provides continuous monitoring of the IV site and was developed on the premise that early detection of an infiltration may help to minimize patient harm.

The device includes a patient monitor, a non-invasive sensor using visible and near-infrared light and a disposable sensor receptacle applied next to the IV site. A color LCD screen displays the status of the IV and an audible notification sounds if an infiltration occurs.

Ten patients were enrolled in a pilot group, giving clinicians an opportunity to perform the protocol and operate the ivWatch device while researchers could make any necessary adjustments prior to starting the next phase of testing.

The second phase of the study is now underway and will enroll 150 patients. This phase will allow researchers to compare the difference between the ivWatch Model 400 and standard nursing practices to detect infiltrations. The final phase of the study will enroll another 150 patients and will allow researchers to estimate the notification rate, infiltration size and severity at early stages of an infiltration.

Hospital nursing staff will assess patients’ PIV sites regularly according to the hospital’s existing protocols. The study protocol does not affect the normal care for the pediatric patient.

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Leah Moore, Director of Marketing, ivWatch, LLC
1.855.489.2824 ext. 7031
Leah.Moore@ivwatch.com