Ignite Creation Date:
2024-05-05 @ 4:59 PM
Last Modification Date:
2024-10-26 @ 9:26 AM
Study NCT ID:
NCT00364416
Status:
COMPLETED
Last Update Posted:
2010-04-28
First Post:
2006-08-11
Brief Title:
Longitudinal Registry for Advanced Heart Failure Patients
Sponsor:
Scios Inc
Organization:
Scios Inc
Study Overview
Official Title:
ADHERE Acute Decompensated Heart Failure National Registry Longitudinal Module-Registry of Advanced Heart Failure Patients at High Risk for Rehospitalization
Status:
COMPLETED
Status Verified Date:
2010-04
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:
The purpose of this study is to gather information to better understand the characteristics medical management techniques and outcomes of patients with chronic severe Heart Failure HF
Detailed Description:
This objectives of this observational registry are to assess changes in patient quality of life as a function of medical management and disease progression as measured by the rate of death and rehospitalization and assist with the optimization of heart failure HF management by providing information on the use of therapies proven to be effective and to describe practices of standard of care for chronic treatment of symptoms of HF outside the hospital and during hospitalization for acute episode with intravenous vasoactive medication drugs which affect the blood vessels and muscle of the heart Additional information which will be gathered include patient characteristics age sex race medical history symptoms infusion setting type of medication dose and frequency of medication and worsening of congestive heart failure disease Participants in the study receive an unique patient-specific identifier and all available data will be analyzed Observational Study - No investigational drug administered
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