We're sorry, but this trial is no longer enrolling volunteers.
The Robotic Vascular and Endovascular Registry (ROVER)
The purpose of the registry is to gather both retrospective and prospective case data on the
use of the commercially available Magellan Robotic System and Magellan Robotic Catheters in
accordance with the approved intended use. For prospective cases, follow-up patient data will
be collected at 14 days (± 5 days) post procedure to assess treatment success, primary
patency of intended targeted vessel region, and adverse events.
The data will be analyzed for medical education, societal presentation, and/or publication by
Over the next 2+ years, physicians who meet the selection criteria will be invited to
participate in the registry.
The objectives of the study are to allow the physician to use the commercially available
Magellan Robotic System and Magellan Robotic Catheters to navigate to the treatment targets
in the peripheral vasculature to:
- Determine the number of endovascular procedures consecutively performed with the
Magellan Robotic System to navigate to treatment targets in the peripheral vasculature
- Achieve stable and efficient system preparation and set-up times, navigation and
cannulation times of target vessels during endovascular procedures, and placement
of therapeutic equipment used to perform endovascular procedures.
- Achieve stable and reduced fluoroscopy time during the endovascular procedures.
- Determine the number of cases required to reach a "steady state," reduction or
predictable time in conducting peripheral interventional procedures using descriptive
(means, ranges) statistics to analyze the data.
This is a prospective and retrospective, multi-center, single arm, non-blinded, sequentially
enrolling data collection activity (for which Hansen Medical is providing funding). Only
patients scheduled to undergo endovascular procedures using the Magellan Robotic System will
be approached for enrollment.
Registry procedures will be conducted in accordance with the labeled indication for use of
the Magellan™ Robotic System.
Prior to the physician participating in the registry and prior to subject enrollment, all
participating physicians will be required to complete Hansen Medical's Magellan Robotic
Participating registry sites must have a commercially available Magellan Robotic System for
the treatment of patients.
Participating sites will be assigned a specific site numeric identification code by the
The information collected into the registry will be data related to the procedure in which
the Magellan System was used or planned to be used and may include patient follow-up data,
minimally 14 days(± 5 days)post procedure but also may include 30 day follow-up to assess for
the resolution of a procedural or post procedure adverse event.
The database will be a repository for the collected registry data and the data will be made
available (in extractable format) to the physician participants.
The data submitted will be reviewed on a regular basis for safety issues and complaints.
Adverse events and/or complaints deemed reportable will be submitted to the appropriate
regulatory agency/agencies by Hansen Medical, Inc.
Inclusion and Exclusion Criteria
- Must be at least 18 years of age;
- Able and willing to provide written informed consent;
- Eligible for minimally invasive or endovascular treatment in the peripheral vasculature;
- Not participating in an investigational study involving the peripheral vasculature.
- Disease targeted for treatment in the coronary vasculature or intra-cerebral vasculature;
- Vasculature that cannot accommodate the Magellan
Please contact Valentina Rodina to learn more about where you can participate in this trial. Please use the contact form on the right side.