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

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00250809
First Posted: November 8, 2005
Last Update Posted: January 7, 2010
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by:
University of New Mexico
  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: Allocation: Non-Randomized
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
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 ]

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:
    Procedure: Placement of a central venous catheter
    Placement of a central venous catheter
  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   Female
Accepts Healthy Volunteers:   No
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
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): 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

Responsible Party: Harriet Smith, MD; Principal Investigator, University of New Mexico - CRTC
ClinicalTrials.gov Identifier: NCT00250809     History of Changes
Other Study ID Numbers: CVC
First Submitted: November 4, 2005
First Posted: November 8, 2005
Last Update Posted: January 7, 2010
Last Verified: March 2009