High-resolution MRI of Atrial Fibrillation Patients Prior to Focal Impulse and Rotor Modulation (FIRM) Ablation
Ohio State University · NCT03444337
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 18+ · All sexes
- Healthy volunteers
- Accepted
- Study type
- Observational
- Target enrollment
- 20
- US sites recruiting
- 1
- Study start
- November 3, 2016
- Record last updated
- September 9, 2026
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
Patients undergoing FIRM guided ablation of atrial fibrillation will undergo high resolution MRI imaging to determine correlation of underlying anatomic fibrotic regions with FIRM targeted sites for ablation.
Being studied: Catheter Ablation
Conditions: Atrial Fibrillation
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Inclusion Criteria
- Patients with symptomatic paroxysmal or persistent atrial fibrillation undergoing clinically-indicated ablation procedure employing FIRM mapping with pre-operative MRI.
- Subjects must be at least 18 years of age.
Exclusion Criteria
- LAA thrombus present on pre-procedure TEE
- Unable to undergo MRI imaging
- Unable to receive gadolinium contrast.
Recruiting US locations
Ohio State University
Columbus, OH 43210
Site contact: Adrianne Miller, MS · 614-688-8252 · Adrianne.Miller3@osumc.edu
Study contacts (from the official record)
- Adrianne Miller, RN · 614-685-4394 · Adrianne.Miller@osumc.edu
- Julie Ryan, RN · 614-685-4394 · julie.ryan@osumc.edu
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