A Randomized Controlled Open Label Trial to Assess the Safety and Efficacy of the OptiVein IV Catheter in an Oncologic Population
Trial Snapshot
- Phase
- Not Applicable
- Status
- Terminated
- Sponsor
- Enrollment
- 109
- Locations
- 2
- Primary Endpoint
- Successful IV insertion on the first attempt
Study Overview
Brief Summary
A prospective, single-center, open-label, randomized controlled trial to assess the safety and efficacy of the OptiVein IV Catheter in an oncology population. The study hypothesis is that OptiVein IV Catheter use will be superior to the control in successful venous access after first attempt.
Detailed Description
The OptiVein IV Catheter is a sterile single use disposable intravascular cannulation device that is modified from CE certified Vasofix Certo Catheter from B.Braun with the additional features of an optical fiber and modified flashplug. The OptiVein System also includes an electronic unit.
The study control and predicate device is the Vasofix Certo IV Catheter from B. Braun Medical Inc. This device is the base device for the OptiVein IV Catheter to which is added the optical fiber and electronic unit.
The OptiVein Catheter shares a similar intended use and the same catheter components as the Vasofix Certo IV Catheter. Clinical data will be obtained to assess if there is a change to the safety and efficacy profile due to the laser component of the OptiVein IV Catheter.
Subject population consists of Oncologic patients who have either difficult to access veins or who have experienced an unsuccessful IV start during their previous visit to the hospital, requiring short-term use of an IV catheter to administer chemotherapy medications intravenously. Subjects may be enrolled multiple times, with each patient-visit being the unit of analysis.
Primary efficacy endpoint is successful IV insertion on the first attempt, defined as placement of the catheter inside the vein allowing for fluid or drug delivery or blood withdrawal.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel
- Primary Purpose
- Supportive Care
- Masking
- None
Eligibility Criteria
- Ages
- 18 Years to — (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •Patients on an ongoing chemotherapy program thru peripheral veins delivery
- •Has difficult to access veins (class II or III) OR has experienced an unsuccessful IV start during his/her previous visit to the hospital
- •Requires peripheral IV therapy (catheter)
- •Has an insertion site in the forearm or hand free of deformities, phlebitis, infiltration, dermatitis, burns, lesions or tattoos
- •Demonstrates cooperation with a catheter insertion and the study protocol
- •Patients 18 years of age or greater
Exclusion Criteria
- •Patients receiving pre-warming of the insertion site
- •Is anesthetized
- •Has a life expectancy of less than one month
- •Transferred from the operating room less than 8 hours post-anasthesia
- •Any patient the research staff deem unobservable
- •The study IV site needs to be immobilized with a splint or other devices
- •Will require a power injection for a radiologic procedure during participation in this study
Arms & Interventions
OptiVein IV catheter
Insertion of an IV catheter into the patient's vein, defined as placement of the catheter inside the vein allowing for fluid or drug delivery or blood withdrawal.
Intervention: Insertion of OptiVein IV catheter (Device)
Vasofix Certo IV catheter
Insertion of an IV catheter into the patient's vein, defined as placement of the catheter inside the vein allowing for fluid or drug delivery or blood withdrawal.
Intervention: Insertion of Vasofix Certo IV catheter (Device)
Outcomes
Primary Outcomes
Successful IV insertion on the first attempt
Time Frame: Immediate
Successful placement of the catheter inside the vein allowing for fluid or drug delivery or blood withdrawal.
Secondary Outcomes
- Incidence of infection(After 72 hours or release from hospital, whichever occurs first.)
- Total number of attempts required for successful IV insertion(Immediate)
- Incidence of fluid extravasation delivered through catheter(Immediate)
- Incidence of blood extravasation resulting in a hematoma(Immediate)
- Time to successful IV insertion(Immediate)
- Unplanned withdrawal of IV catheter(Immediate)