Risk of Central Venous Stenosis in Patients With Chronic Renal Failure After IJ Line Placement
1 other identifier
observational
1,424
1 country
1
Brief Summary
The purpose of this study is to compare the difference in thrombosis as a result of internal jugular (IJ) catheters versus peripherally inserted central catheter (PICC) lines. It is hypothesized that there will be a decreased rate of thrombosis in patients as a result of IJ catheters verses PICC lines.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Oct 2012
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
October 1, 2012
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 1, 2013
CompletedFirst Submitted
Initial submission to the registry
November 13, 2013
CompletedFirst Posted
Study publicly available on registry
November 20, 2013
CompletedStudy Completion
Last participant's last visit for all outcomes
August 1, 2014
CompletedNovember 24, 2014
November 1, 2014
11 months
November 13, 2013
November 20, 2014
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Incidence of Thrombosis
To calculate the incidence of deep venous thrombosis from PICC lines in patients
15 months
Secondary Outcomes (1)
Demographic Risk Factor Association with Risk of Thrombosis from PICC or IJ access
15 months
Study Arms (2)
Thrombosis
incidence of thrombosis in subjects who had PICC line placement
No Thrombosis
no incidence of thrombosis in subjects who had PICC line placement
Eligibility Criteria
Subjects who had a PICC line placed at the University of Chicago by the procedure service between September 1, 2010 and December 31, 2011
You may qualify if:
- subjects who had a PICC line placed at the University of Chicago between September 1, 2010 and December 31, 2011
You may not qualify if:
- subjects under the age of 18
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
The University of Chicago
Chicago, Illinois, 60637, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Mary Hammes, MD
University of Chicago
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
November 13, 2013
First Posted
November 20, 2013
Study Start
October 1, 2012
Primary Completion
September 1, 2013
Study Completion
August 1, 2014
Last Updated
November 24, 2014
Record last verified: 2014-11