Ignite Creation Date:
2024-05-06 @ 4:06 PM
Last Modification Date:
2024-10-26 @ 2:04 PM
Study NCT ID:
NCT04877652
Status:
COMPLETED
Last Update Posted:
2022-05-26
First Post:
2021-04-19
Brief Title:
DR REGISTRY Prospective Observational Study of ADHF Patients With Insufficient Response to Diuretics
Sponsor:
Revamp Medical Ltd
Organization:
Revamp Medical Ltd
Study Overview
Official Title:
DR REGISTRY Prospective Observational Study of Decongestion in Acute Heart Failure Patients With Insufficient Response to Diuretics
Status:
COMPLETED
Status Verified Date:
2022-05
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 study objective is to observe and measure clinical outcomes urine output and safety events occurring during standard medical treatment of ADHF patients deemed to have insufficient diuretic response
Detailed Description:
None
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