Sponsor:
Hartford Hospital
Code:
NCT02095977
Conditions
Implanted With Any Currently (and Any Future) FDA-approved Medtronic ICD or CRT Device
to Which is Attached a St. Jude Riata Lead
Eligibility Criteria
Sex: All
Age: 18+
Healthy Volunteers: Not accepted
Interventions
fluoroscopy
synchronized high-voltage shock
Holter monitor
Brief summary:
Conditions
Implanted With Any Currently (and Any Future) FDA-approved Medtronic ICD or CRT Device
to Which is Attached a St. Jude Riata Lead
Study ID
NCT02095977
Start date
Jul, 2013
Status verified date
Feb, 2017
Completion date
Jan, 2019
Anticipated
Primary completion date
Apr, 2018
Anticipated
Eligibility Criteria
Sex: All
Age: 18+
Healthy Volunteers: Not accepted
Enrollment
30 participants
Anticipated
Intervention Model
Single group
Primary purpose
Screening
Arms
other: participants
Interventions
fluoroscopy
synchronized high-voltage shock
Holter monitor
Primary outcome measure
Central contacts
Locations
Hartford Hospital
Recruiting
Hartford, Connecticut, United States, 06102
Contacts
Principal Investigator:
Steven Zweibel, MD
Sponsor
Hartford Hospital
Last update posted
Feb 8, 2017
Last verified
Feb, 2017
Keywords
Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by Hartford Hospital on 2017-02-08.