Study to Evaluate the Clinical Utility of Radiation Exposure Reduction: Multi-site Rampart Guardian Peripheral Trial

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
AgeNot listed
SponsorBaylor Research Institute

About this trial

Study to Evaluate the Clinical Utility of Radiation Exposure Reduction (SECURE): Multi-site Rampart Guardian Peripheral Trial

Eligibility criteria

Qualifiers

Member of the interventional care team

Elective peripheral procedure

The access site is the femoral artery

The treatment area is at or distal to the iliac artery

Disqualifiers

Individuals who are not yet adults, pregnant women, or prisoners.

Urgent and emergent cases

Trial design

Treatments tested in this trial

  • Rampart IC System

Treatment groups

75 Participants
are divided into 2 treatment groups

Sponsors and collaborators