TroponinT After Subcutaneous Cardioverter-Defibrillator Implantation (TROPIC)

G

German Heart Center Munich

Status

Completed

Conditions

Sudden Cardiac Death

Study type

Observational

Funder types

Other

Identifiers

NCT03526302
GER-EP-018

Details and patient eligibility

About

Serum Troponin levels pre- and postoperatively will be compared in patients receiving an entirely subcutaneous cardioverter-defibrillator.

Full description

To analyze the periprocedural myocardial damage the pre- and postoperative assessment of serum levels of high sensitive TroponinT (hsTnT) is done. The main objectives of the TROPIC register are to evaluate the level of high sensitive TroponinT before and after S-ICD device implantation and to compare these changes in TroponinT-levels with those after standard transvenous ICD-implantation.

Enrollment

43 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Indication for the implantation of an entirely subcutaneous cardioverter-defibrillator

Exclusion criteria

  • None

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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