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Implantable Defibrillator User clinical trials

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NCT ID: NCT03210883 Completed - Heart Failure Clinical Trials

Global Electrical Heterogeneity and Clinical Outcomes

GEHCO
Start date: July 1, 2017
Phase:
Study type: Observational

This retrospective multicenter cohort will validate an independent association of electrocardiographic (ECG) global electrical heterogeneity (GEH) measures with sustained ventricular tachyarrhythmias and appropriate ICD therapies in systolic heart failure patients with primary prevention ICD, and will validate and re-calibrate GEH ECG risk score for prediction of sustained ventricular tachyarrhythmias and appropriate ICD therapies in systolic heart failure patients with primary prevention ICD.

NCT ID: NCT03209726 Completed - Clinical trials for Implantable Defibrillator User

Assessment of S-ICD Eligibility With 12-Lead ECG

EL-SID
Start date: June 21, 2017
Phase:
Study type: Observational

The primary objective of this study is to develop an approach to determine eligibility for subcutaneous ICD by analyzing routine clinical 12-lead electrocardiogram.

NCT ID: NCT03103503 Terminated - Clinical trials for Implantable Defibrillator User

Plexa ICD Lead Registry

Start date: May 18, 2017
Phase:
Study type: Observational [Patient Registry]

The purpose of this registry is to confirm the long-term safety and reliability of BIOTRONIK's Plexa ICD lead.

NCT ID: NCT02976961 Completed - Clinical trials for Implantable Defibrillator User

A Personalized and Interactive Web-based Health Care Innovation to Advance the Quality of Care

ACQUIRE-ICD
Start date: February 6, 2017
Phase: N/A
Study type: Interventional

This study evaluates the clinical efficacy and cost-effectiveness of the ACQUIRE-ICD care innovation as add-on to usual care as compared to usual care alone in patients with an implantable cardioverter defibrillator.

NCT ID: NCT02902458 Completed - Clinical trials for Implantable Defibrillator User

Psychological Intervention modifiEs Outcome of Patients With implAntable Cardioverter dEfibrillator: The PEACE Study

PEACE
Start date: September 2014
Phase: N/A
Study type: Interventional

This study aims to investigate whether follow-up with a psychologist has an impact on the outcome of patients with an implantable automated defibrillator.

NCT ID: NCT02864771 Active, not recruiting - Heart Disease Clinical Trials

Scandinavian Multicenter Study to Advance Risk Stratification in Heart Disease- Ventricular Arrhythmias

SMASH 1
Start date: August 2016
Phase:
Study type: Observational

The purpose of this study is to identify markers of increased risk for incident ventricular arrhythmias and cardiovascular events in patients already being treated with an implantable cardioverter-defibrillator (ICD) by exploring patient history and clinical findings, biological markers, ECG markers, and echocardiographic markers.

NCT ID: NCT02787291 Completed - Clinical trials for Implantable Defibrillator User

A Clinical Evaluation of the Durata or Optisure High Voltage Leads and Ellipse VR ICD Undergoing MRI, an IDE Study

MRI Ready IDE
Start date: May 2016
Phase: N/A
Study type: Interventional

To demonstrate safety and efficacy of the Durata or Optisure high voltage lead and Ellipse VR ICD in an MRI environment.

NCT ID: NCT02491853 Completed - Clinical trials for Implantable Defibrillator User

The Gulf Implantable Cardioverter-Defibrillator Registry

GulfICD
Start date: January 2014
Phase: N/A
Study type: Observational [Patient Registry]

This is a prospective observational multi-center multi-national study of the characteristics and outcomes of patients receiving implantable cardioverter-defibrillators (ICD) in the Arab Gulf region. A total of 1,500 patients will be enrolled. Data on baseline clinical characteristics, ICD programming parameters, inpatient outcomes, and clinical events such as mortality and ICD discharges over 1 year of follow-up will be collected.

NCT ID: NCT02243696 Terminated - Clinical trials for Implantable Defibrillator User

Protego DF4 Post Approval Registry

Start date: September 27, 2014
Phase:
Study type: Observational [Patient Registry]

The purpose of this registry study is to confirm the long-term safety and reliability of the Protego DF4 right ventricular lead.

NCT ID: NCT02232204 Completed - Insomnia Clinical Trials

Sleep and Ventricular Arrhythmias Study

SAVE
Start date: October 2009
Phase: Phase 2
Study type: Interventional

This is a single-center, randomized controlled trial study design. Enrolled participants have a cardiovascular condition for which they are undergoing implantable cardioverter defibrillator (ICD) therapy and comorbid insomnia. Participants were randomized to a behavioral intervention for insomnia in ICD patients or a waitlist control. The treatment intervention period lasted 4 weeks with a telephone booster session administered at 3 month follow-up. The objective of the study is to examine the impact of a brief therapy combining established behavioral approaches to treating insomnia with novel components to target negative cognitions and anxieties associated with cardiac disease and ICD implantation. Primary patient outcomes include sleep, psychological functioning, daytime functioning, cardiac functioning, cognitive performance, and ICD adjustment.