Atrial FibrillationHeart and circulationDevice
What this study is
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.
What's being tested
- Catheter Ablation
Intervention · DEVICE
Study details
- Official title
- High-resolution Contrast-Enhanced MRI of Atrial Fibrillation Patients Prior to FIRM Ablation
- Sponsor
- Ohio State University
- Conditions
- Atrial Fibrillation
- Enrolling
- 20 people
- Starts
- 2016-11-03
- Est. completion
- 2028-04-30
- Record
- View on ClinicalTrials.gov ↗
Who can join
Age 18 Years and overSex ALLHealthy volunteers AcceptedYou may qualify if
- 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.
You can't join if
- LAA thrombus present on pre-procedure TEE
- Unable to undergo MRI imaging
- Unable to receive gadolinium contrast.
Sign in and we'll check these against your records.Full criteria on ClinicalTrials.gov ↗
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1
Study locations (1)
1 openOhio State University
Columbus, Ohio, United States
- Adrianne Miller, MS · Contact614-688-8252Adrianne.Miller3@osumc.edu
- Annie Kellum · Contact614-366-8848Annie.Kellum@osumc.edu
- John Hummel, MD · Principal investigator
- Mahmoud Houmsse, MD · Sub-investigator
- Ralph Augostini, MD · Sub-investigator
- Vadim Fedorov, Phd · Sub-investigator
- Orlando Simonetti, Phd · Sub-investigator
Recruiting
Study team
Sponsor
Ohio State University
Study ID 2016H0200
Study director
Deanna Golden-Kreutz, RN, Phd
Ohio State University
Have questions? The contacts above can answer them before you apply.
Frequently asked questions
The sponsor hasn't published answers to common questions for this trial.