Clinical Trials Directory

Trials / Completed

CompletedNCT03480542

Central Venous Access Study

The CentrAl VenouS Catheter Access DocumEntation (CASCADE) Study

Status
Completed
Phase
Study type
Observational
Enrollment
217 (actual)
Sponsor
Hackensack Meridian Health · Academic / Other
Sex
All
Age
22 Years
Healthy volunteers
Not accepted

Summary

The aim of this study is to document clinicians variation in practice in comparison to standard guidelines by the Medical Center's approved Evidence-based Practice (EBP) guidelines, policies, and procedures for Central Venous Catheter(CVC), Peripherally Inserted Central Catheter (PICC), and Hemodialysis (HD catheters by way of a structured retrospective review of the Electronic Medical Record (EMR) system.

Detailed description

This will be a single site retrospective (non-experimental) study utilizing the electronic medical record, both descriptive and correlational methods. There will be two outcomes: 1. The outcomes associated with the management of Central Venous Catheter(CVC), Peripherally Inserted Central Catheter (PICC), and Hemodialysis (HD) Catheter in adherence with hospital approved Evidence-based Practice guidelines for Central Venous Catheter(CVC), Peripherally Inserted Central Catheter (PICC), and Hemodialysis (HD) Catheter. 2. The mechanical/technical, thrombotic, and other adverse outcomes (Heparin induced coagulopathy) associated with central venous catheters due to variation in insertion and management practices of Central Venous Catheter(CVC), Peripherally Inserted Central Catheter (PICC), and Hemodialysis (HD) Catheter.

Conditions

Timeline

Start date
2017-04-11
Primary completion
2022-04-07
Completion
2022-04-07
First posted
2018-03-29
Last updated
2024-06-10
Results posted
2024-06-10

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT03480542. Inclusion in this directory is not an endorsement.

Central Venous Access Study (NCT03480542) · Clinical Trials Directory