Study Results
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View full resultsBasic Information
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COMPLETED
NA
283 participants
INTERVENTIONAL
2014-06-09
2016-03-17
Brief Summary
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Detailed Description
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Clinical evaluation and device interrogation were performed at baseline, pre- and post-MRI scan, and one month post-MRI for all subjects. At 9-12 weeks post-implant, patients in Cardiac MRI Scan Group underwent an elective non-diagnostic cardiac MRI scan at 1.5 Tesla (T) while patients in Control group underwent device interrogation and clinical evaluation twice with a 45-minute waiting period in between. The safety endpoint was freedom from MRI-related complications while efficacy endpoint was change in right atrial/ ventricular (RA/RV) capture threshold and sensing amplitude from pre-MRI scan to one month post-MRI scan.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
SUPPORTIVE_CARE
NONE
Study Groups
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Cardiac MRI Scan Group
Non-Diagnostic Cardiac MRI scan
Control Group
No interventions assigned to this group
Interventions
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Non-Diagnostic Cardiac MRI scan
Eligibility Criteria
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Inclusion Criteria
* Will receive a new dual chamber pacemaker and leads
* Be willing to undergo an elective MRI scan without complete sedation, that is ,under consciousness during MRI scan
* Be able to provide informed consent for study participation
* Be willing and able to comply with the prescribed follow-up tests and schedule of evaluations
* Is not contraindicated for an MRI scan (per the pre-MRI safety screening form)
* Age≥18 years
* Subjects must be able to undergo pectoral implantation
Exclusion Criteria
* Permanent Atrial Fibrillation/Flutter
* Are medically indicated for an MRI scan at the time of enrollment
* Have an existing active implanted medical device, e.g. neurostimulator, infusion pump etc
* Have a non-MRI compatible device or material implanted
* Have a lead extender or adaptor
* Be unable to fit in MRI bore; will come into contact with the magnet façade inside the MRI bore
* Are currently participating in a clinical investigation that includes an active treatment arm
* Are allergic to dexamethasone sodium phosphate(DSP)
* Are pregnant or planning to become pregnant during the duration of the study
* Have a life expectancy of less than 12 months due to any condition
* Are unable to comply with the follow up schedule
18 Years
ALL
No
Sponsors
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Abbott Medical Devices
INDUSTRY
Responsible Party
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Principal Investigators
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Chi Keong Ching, Dr
Role: PRINCIPAL_INVESTIGATOR
National Heart Center Singapore
Rabindra Nath Chakraborty, Dr
Role: PRINCIPAL_INVESTIGATOR
Apollo Gleneagles Hospital Kolkata India
Locations
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Zhejiang Greentown Cardiovascular Disease Hospital
Hangzhou, , China
Prince of Wales Hospital
Hong Kong, , Hong Kong
Fortis Hospital
Mohali, Punjab, India
Care Institute of Medical Sciences
Ahmedabad, , India
Apollo Hospitals, Bhubaneshwar
Bhubaneshwar, , India
Medanta - The Medicity Hospital
Gurgaon, , India
All India Institute of Medical Sciences, New Delhi
New Delhi, , India
Fortis Escorts Heart Institute and Research Center
New Delhi, , India
Fortis Flt. Lt. Rajan Dhall Hospital
New Delhi, , India
Serdang Hospital
Kajang, , Malaysia
King Chulalongkorn Memorial Hospital
Bangkok, , Thailand
Ramathibodi Hospital
Bangkok, , Thailand
Siriraj Hospital
Bangkok, , Thailand
Countries
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Other Identifiers
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CR-13-031-AP-LV
Identifier Type: -
Identifier Source: org_study_id
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