Clinical Trials Directory

Trials / Terminated

TerminatedNCT00581178

Study to Determine if There Are Specific Clinical Factors to Determine Stent Encrustation

Status
Terminated
Phase
Study type
Observational
Enrollment
16 (actual)
Sponsor
University of California, Irvine · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Ureteral stent placement is one of the most common procedures performed within urology. The stents are generally placed for relief of obstruction or to prevent obstruction following a urological procedure. Most patients with ureteral stents will eventually form stent encrustations. However, patients form these encrustations at dramatically different degrees and rates ranging from no encrustation at 1 year of stenting to severe encrustation in just a few weeks. The purpose of this study is to determine if the degree of encrustation on a stent for any given patient can be predicted based on 24 hour urine parameters prior to stent placement, with the stent in place and after stent removal. Patients who will be receiving stents for other urological reasons will have a 24 hour urine sample collected before stent placement, while the stent is in place and after the stent has been removed. The parameters examined in the 24 hour urine collected will then be compared to the amount of encrustation there is on the stent to see if there is any correlation between the two.

Conditions

Timeline

Start date
2008-04-01
Primary completion
2011-12-01
Completion
2011-12-01
First posted
2007-12-27
Last updated
2013-06-26

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00581178. Inclusion in this directory is not an endorsement.