Advisa MRI Clinical Study
Public ClinicalTrials.gov record NCT01110915. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.
Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.
Official title
Advisa MRI™ System Clinical Investigation
Brief summary
Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.
The purpose of the Advisa MRI System clinical study is to confirm safety and effectiveness in the clinical MRI (Magnetic Resonance Imaging) environment when subjects receive MRI scans up to 2W/kg Specific Absorption Rate (SAR) without positioning restrictions (MRI scans may occur anywhere on the body including the chest).
Study identification
- NCT ID
- NCT01110915
- Recruitment status
- Completed
- Study type
- Interventional
- Phase
- Not applicable
- Enrollment
- 269 participants
Conditions and interventions
Interventions
- Medtronic Advisa MRI Implantable Pulse Generator (IPG) Device
- Medtronic CapSureFix MRI™ active fixation MRI lead Device
Device
Eligibility (public fields only)
- Age range
- Not listed
- Sex
- All
- Healthy volunteers
- Healthy volunteers not accepted
This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.
Study timeline
- Start date
- May 31, 2010
- Primary completion
- Feb 29, 2012
- Completion
- Feb 28, 2013
- Last update posted
- Apr 29, 2013
2010 – 2013
United States locations
- U.S. sites
- 11
- U.S. states
- 11
- U.S. cities
- 11
| Facility | City | State | ZIP | Site status |
|---|---|---|---|---|
| Central Coast Cardiology | Salinas | California | 93901-3901 | — |
| Mid Florida Cardiology | Orlando | Florida | 32806-2014 | — |
| Iowa Heart Center | West Des Moines | Iowa | 50266 | — |
| Mid America Heart Institute | Kansas City | Missouri | 64111 | — |
| Raleigh Cardiology Associates | Raleigh | North Carolina | 27610 | — |
| The Lindner Research Center | Cincinnati | Ohio | 45219-2906 | — |
| Oklahoma Heart Institute | Tulsa | Oklahoma | 74104 | — |
| Greenville Hospital System | Greenville | South Carolina | 29605 | — |
| Cardiology Associates of East Tennesee | Knoxville | Tennessee | 37923-4310 | — |
| Baylor Heart & Vascular Hosptial | Dallas | Texas | 75226-1300 | — |
| University of Virginia Health System | Charlottesville | Virginia | 22908-0816 | — |
Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.
Non-U.S. locations
This page focuses on the U.S. directory. The official record also lists 26 non-U.S. sites.
About this trial record page
- What this page shows
- Public field values for ClinicalTrials.gov record NCT01110915, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
- What this page does not do
- No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
- Where the data comes from
- Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
- Last refresh
- Last update posted Apr 29, 2013 · Synced Sep 2, 2026
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Open the official record
The complete protocol, eligibility criteria, and contact information for NCT01110915 live on ClinicalTrials.gov.