Ignite Creation Date:
2024-05-06 @ 6:23 PM
Last Modification Date:
2024-10-26 @ 2:47 PM
Study NCT ID:
NCT05642650
Status:
NOT_YET_RECRUITING
Last Update Posted:
2023-02-08
First Post:
2022-11-15
Brief Title:
Novel Wearable Device for Heart Failure Management
Sponsor:
China-Japan Friendship Hospital
Organization:
China-Japan Friendship Hospital
Study Overview
Official Title:
Clinical Translational Research of Novel Wearable Device Based on Patented Sensing Technology in Non-Invasive Management of Heart Failure
Status:
NOT_YET_RECRUITING
Status Verified Date:
2023-02
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
Heart failure HF is a major cardiovascular disease with high readmission and mortality rate A wearable device that could remotely monitor and detect the worsening HF early before the symptoms appear will help reduce HF readmissions effectively The purpose of the current study is to examine the efficiency of a novel wearable device based on flexible strain sensor comparing to the clinical gold standard and then transform it into a clinical application
Detailed Description:
The prospective cohort study aims to examine the efficiency of a novel wearable device based on a flexible strain sensor to improve the outcomes of patients with HF compared to the standard-of-care without wearable device monitoring
The primary and secondary endpoints will be examined in subgroups determined by baseline variables reflecting demographyNYHA functional classleft ventricular ejection fractionnatriuretic peptideadditional co-morbiditiesand others
The primary and secondary endpoints will be examined in subgroups determined by baseline variables reflecting demographyNYHA functional classleft ventricular ejection fractionnatriuretic peptideadditional co-morbiditiesand others
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None