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Evaluation of Novel Biomarkers to Improve Risk Stratification and Patient Selection in Implantable Cardioverter-defibrillator (ICD) Therapy

Evaluation of Novel Biomarkers to Improve Risk Stratification and Patient Selection in ICD Therapy

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01594073
Acronym
BIOMARKERICD
Enrollment
500
Registered
2012-05-08
Start date
2012-04-30
Completion date
Unknown
Last updated
2021-02-11

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

Conditions

Cardiac Death, Ventricular Arrhythmias

Keywords

implantable defibrillator, ventricular arrhythmias, cardiac death

Brief summary

Implantable cardioverter-defibrillator (ICD) therapy reduces mortality in patients with chronic heart failure and reduced left ventricular ejection fraction (LVEF) \<36%. Nevertheless, patient selection for ICD therapy based on LVEF and NYHA functional class alone seems to have a low specificity and sensitivity: In 100 patients treated, the SCD-HeFT study prevented 7 deaths in 5 years. Therefore 93 patients have a risk of adverse effects, such as operation risk, infection, pneumothorax, lead dislocation, and inadequate icd therapy. On the other hand, patients with advanced or end stage heart failure might rather die off progressive heart failure death and thus not benefit from ICD therapy. It therefore seems appropriate and necessary to improve the individualized risk stratification in these patients. The aim of this study is to evaluate multiple cardiac biomarkers in a model predicting ventricular arrhythmias in patients on ICD therapy.

Detailed description

Patients having or getting an ICD in the Dept. of Cardiovascular Medicine of the Hannover Medical School will be recruited in the next 2 years. Blood samples of all patients will be obtained at inclusion and at 6 months follow-up. Patients will be followed-up for 1-2 years after inclusion.

Interventions

None listed

Sponsors

Hannover Medical School
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

* Patient meeting the current indications for primary or secondary prophylactic ICD/CRT-D therapy * age 18 years or older

Exclusion criteria

* Patient unwilling to participate.

Design outcomes

Primary

MeasureTime frameDescription
ICD therapy2 yearsICD therapy (ATP/Shock) for ventricular fibrillation/ventricular tachycardia or inadequate therapy for supraventricular tachycardia/oversensing/lead dysfunction

Secondary

MeasureTime frameDescription
Depression scale2 yearsPHQ-9
6-Minute-walk-test6 months6-Minute-walk-test
Quality of life2 yearsMLWHFQ, EQ5D
Heart Failure Events2 yearsChanges in NYHA classification, Hospitalizations
Risc Scores for Heart Failure events/ICD therapy2 yearsSeattle Heart Failure Model, Lee-Score, PROFIT-Score
all-cause mortality2 yearsAll-cause mortality

Countries

Germany

Outcome results

None listed

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