Ignite Creation Date:
2024-10-26 @ 3:43 PM
Last Modification Date:
2024-10-26 @ 3:43 PM
Study NCT ID:
NCT06654232
Status:
NOT_YET_RECRUITING
Last Update Posted:
None
First Post:
2024-10-21
Brief Title:
Patient-Reported Quality of Life in Patients with an Implantable-Cardioverter Defibrillator - a Cross-Sectional Observational Study
Sponsor:
None
Organization:
None
Study Overview
Official Title:
Patient-Reported Quality of Life in Patients with an Implantable-Cardioverter Defibrillator - a Cross-Sectional Observational Study
Status:
NOT_YET_RECRUITING
Status Verified Date:
2024-10
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
No
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
QoL-ICD I
Brief Summary:
Patients at risk for life-threatening arrhythmias are eligible for the implantation of an implantable cardioverter-defibrillator ICD which has repeatedly shown improved survival However living with an ICD may pose several challenges and affect quality of life QoL This prospective cross-sectional observational cohort studies will provide detailed insights in patient-reported QoL The aim is to study the QoL perspective of patients who have an ICD including physical and emotional health ICD acceptance concerns of ICD patients with regard to physical and sexual activity
Detailed Description:
None
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None