Strategic MAnagement to Optimize Response To Cardiac Resynchronization Therapy Registry
Status: | Recruiting |
---|---|
Conditions: | Cardiology |
Therapuetic Areas: | Cardiology / Vascular Diseases |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 3/8/2019 |
Start Date: | April 14, 2017 |
End Date: | August 1, 2022 |
Contact: | Sara Veraghtert |
Email: | sara.veraghtert@bsci.com |
Phone: | +32(0)478783897 |
Strategic MAnagement to Optimize Response To Cardiac Resynchronization Therapy Registry (SMART Registry)
To learn in a general Cardiac Resynchronization Therapy Defibrillators (CRT-D) population,
which optimization techniques are used and how effective they are. It will compare 12-month
response rates among different optimization methods and characterize which selected subject
subgroups achieve better response than others.
A subset of SMART Registry subjects will contribute to the NG4 Post Market Clinical Follow Up
(PMCF) Cohort whose objective is collecting data on the NG4 CRT-D features and device usage
in a real world setting and monitor long term safety associated with these devices to support
CE Mark.
which optimization techniques are used and how effective they are. It will compare 12-month
response rates among different optimization methods and characterize which selected subject
subgroups achieve better response than others.
A subset of SMART Registry subjects will contribute to the NG4 Post Market Clinical Follow Up
(PMCF) Cohort whose objective is collecting data on the NG4 CRT-D features and device usage
in a real world setting and monitor long term safety associated with these devices to support
CE Mark.
Inclusion Criteria:
- Subject implanted or upgraded with a NG3 or NG4 CRT-D device connected with any
manufacturer quadripolar LV lead based on BSC labeling for devices in specific
geographies.
- Subjects must be enrolled between 1 and 21 calendar days post CRT-D implantation
procedure.
- Subject is age 18 or above, or of legal age to give informed consent specific to each
country and national laws
- Subject is willing and capable of complying with follow-up visits and procedures as
defined by this protocol
Exclusion Criteria:
- Subject with documented life expectancy of less than 12 months
- Subject currently on the active heart transplant list or has a current Left
Ventricular Assist Device or other assist device (mechanical circulatory support
device).
- Subject who have had a pre-existing CRT device
- Subject enrolled in any other concurrent clinical trial without prior written approval
from BSC Clinical Trial Manager
- Women of childbearing potential who are or might be pregnant at time of study
enrolment
- Any contra-indication to receive a CRT-D device per local guidelines
We found this trial at
31
sites
3535 Southern Blvd
Kettering, Ohio 45429
Kettering, Ohio 45429
(937) 298-4331
Principal Investigator: Khawaja Shahid H Baig, Dr.
Kettering Medical Center Our flagship hospital, Kettering Medical Center, stands proudly in Kettering, Ohio. From...
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931 S. 9th Street
Bismarck, North Dakota 58504
Bismarck, North Dakota 58504
701-530-6954
Principal Investigator: Colby Halsy, Dr
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Gainesville, Florida 32608
Principal Investigator: Mark Panna, Dr.
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1200 Old York Road
Abington, Pennsylvania 19001
Abington, Pennsylvania 19001
(215) 481–2000
Principal Investigator: Charles Gottlieb, Dr.
Abington Memorial Hospital Abington Memorial Hospital (AMH) is a 665-bed, regional referral center and teaching...
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3831 Piper Street
Anchorage, Alaska 99508
Anchorage, Alaska 99508
Principal Investigator: Steve Compton, Dr.
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Bakersfield, California 93309
Principal Investigator: Moksedul Habib, Dr
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2401 W Belvedere Ave
Baltimore, Maryland 21215
Baltimore, Maryland 21215
(410) 601-9000
Principal Investigator: Mohammed Kanjwal, Dr
Sinai Hospital of Baltimore Sinai Hospital of Baltimore provides a broad array of high-quality, cost-effective...
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Bedford Park, South Australia 5042
Principal Investigator: Andrew McGavin, Dr.
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Brandon, Florida 33511
Principal Investigator: Stephen Mester, Dr.
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3050 Orchard Park Road
Buffalo, New York 14215
Buffalo, New York 14215
Principal Investigator: Prajwal Deshmukh, Dr.
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Chicago, Illinois 60612
Principal Investigator: Erik Wissner, Dr
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Danbury, Connecticut 06810
Principal Investigator: Robert Winslow, Dr.
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Davenport, Iowa 52803
Principal Investigator: Linda Hu, Dr.
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350 N Wall St
Kankakee, Illinois 60901
Kankakee, Illinois 60901
Principal Investigator: Brad Supernant, Dr.
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Lafayette, Louisiana 70506
Principal Investigator: Marc Saad, Dr.
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New York, New York 10032
Principal Investigator: Jose Dizon, Dr.
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416 Connable Avenue
Petoskey, Michigan 49770
Petoskey, Michigan 49770
Principal Investigator: Daniel Buerkel, Dr.
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Richmond, Virginia 23249
Principal Investigator: Karoly Kaszala, Dr.
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Salisbury, Maryland 21804
Principal Investigator: Nsah Emmanuel, Dr.
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Washington, Pennsylvania 15301
Principal Investigator: Maninder Bedi, Dr.
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Wilmington, North Carolina 28401
Principal Investigator: Meena Rao
Phone: 910-667-4044
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