Scheduled Triple-Lumen Central Venous Catheter Exchange: A Prospective Controlled Randomized Study

This study has been completed.

First Received: November 4, 2005 Last Updated: March 26, 2009 History of Changes

Sponsored by:	University of New Mexico
Information provided by:	University of New Mexico
ClinicalTrials.gov Identifier:	NCT00250809

Purpose

CVC Pros and Cons of scheduled Triple-lumen Central Venous Catheter Exchange: A Prospective Controlled Randomized Study

Condition	Intervention
Other Female Genital Cancer	Procedure: Placement of a central venous catheter

Study Type:	Interventional
Study Design:	Treatment, Non-Randomized, Open Label, Uncontrolled, Single Group Assignment
Official Title:	CVC Pros and Cons of Scheduled Triple-Lumen Central Venous Catheter Exchange: A Prospective Controlled Randomized Study

Further study details as provided by University of New Mexico:

Primary Outcome Measures:

Pros and Cons of scheduled Triple-lumen Central Venous Catheter Exchange [ Time Frame: 3 years ] [ Designated as safety issue: Yes ]

Enrollment:	15
Study Start Date:	March 1994
Study Completion Date:	March 2006
Primary Completion Date:	December 2005 (Final data collection date for primary outcome measure)

Intervention Details:

Placement of a central venous catheter

Eligibility

Criteria

Inclusion Criteria:

1. Patients who require the placement of a central venous catheter for medical purposes and have an absence of infection.

Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00250809

Locations

United States, New Mexico
University of New Mexico
Albuquerque, New Mexico, United States, 87131

Sponsors and Collaborators

University of New Mexico

Investigators

Principal Investigator:

Harriet Smith, MD

University of New Mexico

More Information

No publications provided

Responsible Party:	University of New Mexico - CRTC ( Harriet Smith, MD; Principal Investigator )
Study ID Numbers:	CVC
Study First Received:	November 4, 2005
Last Updated:	March 26, 2009
ClinicalTrials.gov Identifier:	NCT00250809 History of Changes
Health Authority:	United States: Institutional Review Board

ClinicalTrials.gov processed this record on September 10, 2009