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Clinical Trials/NCT00581178
NCT00581178
Terminated
Not Applicable

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

University of California, Irvine1 site in 1 country16 target enrollmentApril 2008
ConditionsKidney Stones

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Kidney Stones
Sponsor
University of California, Irvine
Enrollment
16
Locations
1
Status
Terminated
Last Updated
12 years ago

Overview

Brief 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.

Registry
clinicaltrials.gov
Start Date
April 2008
End Date
December 2011
Last Updated
12 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Victor Huynh

Urology Account Contact

University of California, Irvine

Eligibility Criteria

Inclusion Criteria

  • Patient at UCI
  • Scheduled to undergo surgery (standard of care) where ureteral stent will be placed

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Not specified

Study Sites (1)

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