Radiation-Exposure Reduction in Peripheral Procedures using Rampart IC System
Official title: Study to Evaluate the Clinical Utility of Radiation Exposure Reduction (SECURE): Multi-site Rampart Guardian Peripheral Trial
Run by Baylor Research Institute · NCT07467720 · Data updated 2026-11-12
This study tests whether using the Rampart IC System during elective femoral-artery access peripheral procedures reduces radiation exposure for patients.
Quick facts
| Study type | Interventional |
|---|---|
| Sex | All |
| Enrollment | 75 (estimated) |
| Sponsor | Baylor Research Institute Academic / other |
| Drugs / interventions | Radiation |
| Locations | 1 site (Plano, Texas) |
| Status | Recruiting |
| Started | August 20, 2026 |
| Main results expected | May 15, 2027 |
| Study ends | May 15, 2027 |
| Registry record updated | August 21, 2026 |
| Trial ID | NCT07467720 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults involved in elective peripheral procedures with femoral access and treatment area at or distal to the iliac artery, who are part of the interventional care team.
✕Probably not a fit
Patients undergoing urgent/emergent procedures or those not meeting the inclusion criteria may not benefit from the Rampart IC System in this context.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This investigator-initiated, prospective, randomized study is conducted across multiple sites to determine the clinical utility of reducing radiation exposure with the Rampart IC System during elective peripheral interventions. Eligible teams performing femoral-access procedures compare standard practice to the Rampart IC System, assessing radiation exposure and related outcomes. The trial excludes pediatric, pregnant, and prison populations, and does not include urgent or emergent cases. Baylor Research Institute leads the study with Baylor Scott & White The Heart Hospital–Plano as the site.
Why it matters
Potential benefit: If successful, patients could experience lower radiation exposure during certain peripheral procedures.
How similar studies have gone: Previous similar approaches in radiation reduction have shown promise in interventional settings, supporting exploration of Rampart IC System here.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * 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 Exclusion Criteria: * Individuals who are not yet adults, pregnant women, or prisoners. * Urgent and emergent cases
Where it's running
-
Baylor Scott & White The Heart Hospital- Plano
Plano, Texas, United States Recruiting
Study contacts
- Study coordinator: Bonnie Ostergren
- Email: bonnie.ostergren@bswhealth.org
- Phone: 469-814-4181
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.