Status:
RECRUITING
Deimplementing CXR After CVC (DRAUP) in the ICU
Lead Sponsor:
Washington University School of Medicine
Collaborating Sponsors:
National Heart, Lung, and Blood Institute (NHLBI)
Conditions:
Implementation Science
Behavior and Behavior Mechanisms
Eligibility:
All Genders
18+ years
Phase:
NA
Brief Summary
This study proposes adapting and testing an innovative, behavioral theory-driven deimplementation program called DRAUP in two intensive care units for proof of concept and support that the program can...
Detailed Description
There are millions of critically ill patients annually who require imaging confirmation after central venous catheter insertion. Emerging literature demonstrates that ultrasound is a faster alternativ...
Eligibility Criteria
Inclusion
- Measure the effectiveness and cost effectiveness of DRAUP on discontinuation of CXRs
- Inclusion Criteria for DRAUP training:
- (1) ICU faculty, fellows, senior residents (post graduate year 3) and advanced practice practitioners
- ICU inclusion for DRAUP program:
- Availability of ultrasound machines with archiving capability (DICOM)
- A minimum of 100 supradiaphragmatic CVC insertions annually in adult patients (age \>18)
- Capacity to access digital archiving (PICOM)
- Patient inclusion for DRAUP program:
- supradiaphragmatic CVC placed
- Patient exclusion for DRAUP program:
- severe instability (cardiac arrest, severe shock) where CVC would be used without CXR,
- level 1 trauma;
- burn patients with no viable skin surface for imaging
Exclusion
Key Trial Info
Start Date :
January 2 2024
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
December 31 2025
Estimated Enrollment :
100 Patients enrolled
Trial Details
Trial ID
NCT06146348
Start Date
January 2 2024
End Date
December 31 2025
Last Update
March 12 2025
Active Locations (1)
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1
Washington University School of Medicine
St Louis, Missouri, United States, 63108