Arteriovenous Fistula Tissue Bank

The recruitment status of this study is unknown because the information has not been verified recently.
Verified July 2010 by University of Nebraska.
Recruitment status was  Recruiting
Sponsor:
Information provided by:
University of Nebraska
ClinicalTrials.gov Identifier:
NCT00836862
First received: February 3, 2009
Last updated: July 15, 2010
Last verified: July 2010

February 3, 2009
July 15, 2010
February 2009
November 2011   (final data collection date for primary outcome measure)
Not Provided
Not Provided
Complete list of historical versions of study NCT00836862 on ClinicalTrials.gov Archive Site
Not Provided
Not Provided
Not Provided
Not Provided
 
Arteriovenous Fistula Tissue Bank
Arteriovenous Fistula Tissue Bank

This project will bank sera, DNA and vascular specimens from patients undergoing arteriovenous fistula creation and revision

Not Provided
Observational
Time Perspective: Prospective
Not Provided
Retention:   Samples With DNA
Description:

Serum, Whole Blood, Tissue

Probability Sample

Patients will be eligible if they are 19 years of age or greater and have placement of an arteriovenous fistula planned witin 30 days.

Kidney Failure, Chronic
Other: Biologic specimens
Banking of serum, DNA and tissue
Arteriovenous Fistula
Intervention: Other: Biologic specimens
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruiting
50
Not Provided
November 2011   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • Age 19 years of age or greater
  • Arteriovenous fistula placement for hemodialysis access scheduled within 30 days

Exclusion Criteria:

  • Incompetent to provide informed consent
Both
19 Years and older
No
Not Provided
United States
 
NCT00836862
482-08-EP
No
Troy J. Plumb, MD, University of Nebraska Medical Center
University of Nebraska
Not Provided
Not Provided
University of Nebraska
July 2010

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP