Accent Cardiac MRI Study

NCT ID: NCT02041702

Last Updated: 2019-08-21

Study Results

Results available

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Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

283 participants

Study Classification

INTERVENTIONAL

Study Start Date

2014-06-09

Study Completion Date

2016-03-17

Brief Summary

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The aim of this study was to assess safety and efficacy of SJM MRI conditional pacing system. The study hypothesized that cardiac MRI scan would not affect performance of SJM MRI conditional pacing system.

Detailed Description

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Accent Cardiac MRI study was a prospective, randomized ,multi-center study conducted in Asia. Subjects indicated for dual-chamber pacemaker and who signed study consent form were considered enrolled and post implant were randomized to either Cardiac MRI Scan Group or Control Group.

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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Bradycardia

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Participants are assigned to one of two groups in parallel for the duration of the study
Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

NONE

Study Groups

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Cardiac MRI Scan Group

Group Type EXPERIMENTAL

Non-Diagnostic Cardiac MRI scan

Intervention Type DIAGNOSTIC_TEST

Control Group

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Non-Diagnostic Cardiac MRI scan

Intervention Type DIAGNOSTIC_TEST

Eligibility Criteria

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Inclusion Criteria

* Have an approved indication per American College of Cardiology(ACC)/ American Heart Association(AHA)/ Heart Rhythm Society(HRS)/ European Society of Cardiology(ESC) guidelines for implantation of a pacemaker
* 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

* Having an existing pacemaker or Implantable Cardioverter Defibrillator (ICD) .A new pacemaker and lead is required for enrollment
* 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
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Abbott Medical Devices

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

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

Site Status

Prince of Wales Hospital

Hong Kong, , Hong Kong

Site Status

Fortis Hospital

Mohali, Punjab, India

Site Status

Care Institute of Medical Sciences

Ahmedabad, , India

Site Status

Apollo Hospitals, Bhubaneshwar

Bhubaneshwar, , India

Site Status

Medanta - The Medicity Hospital

Gurgaon, , India

Site Status

All India Institute of Medical Sciences, New Delhi

New Delhi, , India

Site Status

Fortis Escorts Heart Institute and Research Center

New Delhi, , India

Site Status

Fortis Flt. Lt. Rajan Dhall Hospital

New Delhi, , India

Site Status

Serdang Hospital

Kajang, , Malaysia

Site Status

King Chulalongkorn Memorial Hospital

Bangkok, , Thailand

Site Status

Ramathibodi Hospital

Bangkok, , Thailand

Site Status

Siriraj Hospital

Bangkok, , Thailand

Site Status

Countries

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China Hong Kong India Malaysia Thailand

Other Identifiers

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CR-13-031-AP-LV

Identifier Type: -

Identifier Source: org_study_id

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