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Myocardial Minimal Damage After Rapid Ventricular Pacing

Myocardial Minimal Damage After Rapid Ventricular Pacing

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02362802
Acronym
MyDate
Enrollment
149
Registered
2015-02-13
Start date
2014-09-30
Completion date
2018-01-31
Last updated
2023-03-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Antitachycardia Pacing

Brief summary

This study aims to investigate the impact of antitachycardia pacing ( ATP) on the myocardial tissue with respect to its potential micro damage measured by several myocardial markers, especially by high-sensitive TroponinT.

Interventions

DEVICEImplantable Cardioverter Defibrillator

Sponsors

Deutsches Herzzentrum Muenchen
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* All patients for de-novo implantation of a transvenous ICD (single chamber, dual chamber or cardiac resynchronization tehrapy) with left pectoral device position and planned apical location of the right ventricular defibrillation electrode.

Exclusion criteria

* Resuscitation, cardiac surgical procedure, acute coronary syndrome, acute myocardial infarction, coronary revascularisation, cardioversion or ablation during the past 4 weeks, if baseline high-sensitive Troponin T is elevated * Known stenosis of coronary vessels with indication for coronary intervention or operative revascularisation * Intracardiac thrombus or general contraindication against ventricular burst stimulation or intraoperative ICD-testing * Atypical lead implantation with indication for defibrillation threshold testing by induction of ventricular fibrillation * Right sided implantation of ICD * Planned electrical cardioversion * Lead explantation or -extraction during procedure * Redo procedure (except of additional implantation of a right ventricular ICD lead) * Present temporary pacemaker electrode * ASA \>= IV or NYHA IV * Cardiogenic shock * Pulmonary embolism, cerebrovascular insult or dialysis in the past 4 weeks * Lack of consent of patient * Minority of patient

Design outcomes

Primary

MeasureTime frame
High sensitive Troponin14-20 hours

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026