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Clinical Trial Details

Study Title: Longitudinal Surveillance Registry (LSR) of ACUITY Spiral
Study Type: Observation
Study Condition: Heart Failure
Investigator: Dr. Mark Landers
Phone: (910) 715-8600
Research Coordinator: Anne Dickerson
Phone: (910) 715-2200
Eligibility Criteria: Men or women who have been or will be implanted with the ACUITY Spiral Lead. For additional criteria, call the Research Coordinator or visit the study weblink.
Sponsor Organization: Boston Scientific Corporation
Study Rationale: The primary purpose of the LSR of ACUITY Spiral is to evaluate and report on the long-term performance of the ACUITY Spiral LV Lead.
Study Purpose:
Study Link: http://clinicaltrials.gov/ct2/show/NCT00955708
   
 
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