Rampart IC System for Radiation Shielding

(SECURE Trial)

BO
Overseen ByBonnie Ostergren
Age: Any Age
Sex: Any
Trial Phase: Academic
Sponsor: Baylor Research Institute
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

What You Need to Know Before You Apply

What is the purpose of this trial?

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

Are You a Good Fit for This Trial?

Inclusion Criteria

My procedure uses the femoral artery as the access site.
* Member of the interventional care team
I am scheduled for a planned minor procedure on my limbs or extremities.
See 1 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Intraprocedural

Participants undergo procedures with either traditional lead aprons and shields or the Rampart IC System to evaluate radiation exposure reduction

Intraprocedural

Follow-up

Participants are monitored for safety and effectiveness after the procedures

4 weeks

What Are the Treatments Tested in This Trial?

Interventions

  • Rampart IC System

How Is the Trial Designed?

2

Treatment groups

Active Control

Group I: Traditional Lead Apron and ShieldsActive Control1 Intervention
Group II: Rampart IC SystemActive Control1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

Baylor Research Institute

Lead Sponsor

Trials
210
Recruited
205,000+