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SJM MRI Diagnostic Imaging Registry (IDE)
NCT02807948 · View on ClinicalTrials.gov ↗
Study Summary
This study is a prospective, non-randomized, multi-center study of subjects implanted with an SJM pacemakers, implantable cardioverter defibrillator (ICD), and cardiac resynchronization therapy (CRT) devices who are clinically indicated for a non-thoracic MRI scan.
Conditions Studied
Interventions
- DEVICE Pacemaker, ICD, or CRT device
Study Locations (20)
California
- Quest Imaging — Bakersfield
- Raymond Schaerf, MD — Burbank
- John Muir Medical Center — Concord
- St. Helena Hospital — Deer Park
- Cardiovascular Consultants Heart Center — Fresno
- Newport Diagnostic Center — Newport Beach
- Pro Health Advance Imaging — North Hollywood
- Eisenhower Medical Center — Rancho Mirage
- St. Mary's Medical Center — San Francisco
- Sansum Clinic - Santa Barbara Medical Foundation — Santa Barbara
Florida
- Cardiac Arrhythmia Services — Boca Raton
- Jupiter Medical Center — Jupiter
- Florida Hospital — Orlando
Arizona
- Scottsdale Medical Imaging — Scottsdale
- University of Arizona — Tucson
Colorado
- South Denver Cardiology Associates PC — Littleton
- Medical Center of the Rockies — Loveland
Arkansas
- St. Bernards — Jonesboro
Connecticut
- Hartford Hospital — Hartford
Delaware
- Christiana Hospital — Newark
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 189 participants |
| Start Date | 2016-06 |
| Est. Completion | 2018-01-31 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02807948
The ClinicalTrials.gov registry entry for NCT02807948 describes a study currently listed as completed. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 189 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Abbott Medical Devices, which has 155 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with Cardiac Arrhythmia appearing as the primary indexed condition, and to 1 intervention — of which Pacemaker, ICD, or CRT device is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT02807948 reports 20 study locations spanning 7 distinct geographic areas — top geographies include California, Florida, Arizona. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT02807948 about?
NCT02807948 is a clinical study titled "SJM MRI Diagnostic Imaging Registry (IDE)". This study is a prospective, non-randomized, multi-center study of subjects implanted with an SJM pacemakers, implantable cardioverter defibrillator (ICD), and cardiac resynchronization therapy (CRT) devices who are clinically indicated for a non-thoracic MRI scan.
What is the current status of trial NCT02807948?
This trial is currently completed. It is a NA study. The enrollment target is 189 participants. The study started on 2016-06. Estimated completion is 2018-01-31.
What conditions does trial NCT02807948 study?
This clinical trial studies the following conditions: Cardiac Arrhythmia. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT02807948?
The interventions under investigation include: Pacemaker, ICD, or CRT device (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT02807948?
This trial is sponsored by Abbott Medical Devices, which has 155 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT02807948 being conducted?
This trial has 20 study locations across Arizona, Arkansas, California, Colorado, Connecticut. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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