Viewing Study NCT06373575



Ignite Creation Date: 2024-05-06 @ 8:24 PM
Last Modification Date: 2024-10-26 @ 3:27 PM
Study NCT ID: NCT06373575
Status: ENROLLING_BY_INVITATION
Last Update Posted: 2024-04-18
First Post: 2024-04-10

Brief Title: IVC and Lung Ultrasound B-lines Guided Decongestion in Critically Ill ESKD Patients With Heart Failure
Sponsor: The First Affiliated Hospital with Nanjing Medical University
Organization: The First Affiliated Hospital with Nanjing Medical University

Study Overview

Official Title: Inferior Vena Cava and Lung Ultrasound B-lines Guided Decongestion in Critically Ill Kidney Failure Patients With Heart Failure a Single-center Prospective Randomized Controlled Intervention Study
Status: ENROLLING_BY_INVITATION
Status Verified Date: 2024-04
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 objectives of this trial are to determine whether in critically ill ESKD patients randomization to fluid removal guided by lung and inferior vena cava ultrasound compared to standard care leads to Improved pulmonary congestion primary outcome and safety secondary outcome in the short-term
Detailed Description: The point-of-care ultrasound was thought useful in the management of fluid in critically ill patients At present the role of the lung and inferior vena cava ultrasound is unclear in the management of decongestion of heart failure in kidney failure KF patients using prolonged hemodialysis The investigators aim to explore the effect of pre-dialysis probing with the lung and inferior vena cava to guide fluid removal as compared with conventional protocols on the improvement of heart failure symptoms in patients with KF with heart failure under prolonged hemodialysis in the short-term

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