No registrations found.
ID
Source
Brief title
Health condition
Pacemaker and ICD implantation
High-sensitive troponin T
Myocardial damage
Sponsors and support
Intervention
Outcome measures
Primary outcome
The value of high-sensitive troponin T after pacemaker or ICD implantation.
The study endpoint is reached after a follow-up period of 6 months unless an acute myocardial infarction occurs before that moment
Secondary outcome
Patient and procedural characteristics that might influence the outcome of the main study parameter
Background summary
To examine the range of values of hsTnT between patients after implantation of a device ((bi-ventricular) ICD or pacemaker (PM)) in order to define new hsTnT reference values.
Study objective
Within 24hours after implantation, high-sensitive troponin T is elevated as a result of myocardial damge
Study design
Between 12 and 24 hours prior to device implantation, one blood sample will be taken.
In addition, 3, 6 and 24 hours after device implantation new blood samples will be obtained
Intervention
In each patient, 4 blood samples will be taken
N.M.S. Groot, de
Erasmus MC, afdeling Cardiologie, Kamer BA-579
Rotterdam 3015 CE
The Netherlands
+31 (0)10 7034479
n.m.s.degroot@erasmusmc.nl
N.M.S. Groot, de
Erasmus MC, afdeling Cardiologie, Kamer BA-579
Rotterdam 3015 CE
The Netherlands
+31 (0)10 7034479
n.m.s.degroot@erasmusmc.nl
Inclusion criteria
Adults scheduled for pacemaker of ICD implantation
Exclusion criteria
Mental disability
Acute myocardial infarction <30 days before implantation
Congenital heart defects
Design
Recruitment
Followed up by the following (possibly more current) registration
No registrations found.
Other (possibly less up-to-date) registrations in this register
No registrations found.
In other registers
Register | ID |
---|---|
NTR-new | NL4500 |
NTR-old | NTR4676 |
Other | Erasmus MC : METC |