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
	
								Bedford Park, South Australia 5042			
	
			
					Principal Investigator: Andrew McGavin, Dr.
			
						
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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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								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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									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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								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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