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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06384079
Other study ID # STU00219828
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date May 2024
Est. completion date November 2030

Study information

Verified date April 2024
Source Northwestern University
Contact Emily Ji
Phone 312-695-8146
Email emily.ji@nm.org
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Our objective is to assess the effect of duration of ureteral rest, defined as time from conversion of ureteral stent to percutaneous nephrostomy, on stricture length prior to ureteral reconstruction surgery.


Recruitment information / eligibility

Status Recruiting
Enrollment 25
Est. completion date November 2030
Est. primary completion date November 2025
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - >18 years of age - Undergoing ureteral reconstruction surgery for ureteral stricture with conversion of an indwelling stent to a percutaneous nephrostomy tube for ureteral rest - Willing to sign informed consent form - Able to read and understand informed consent form Exclusion Criteria: - <18 years of age - Inability to provide informed consent - Members of vulnerable patient populations

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Antegrade and retrograde pyelogram
Participation in the study will guarantee that participants will receive this procedure.

Locations

Country Name City State
United States Northwestern University Chicago Illinois

Sponsors (1)

Lead Sponsor Collaborator
Northwestern University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Ureteral stricture length measured by antegrade or retrograde pyelogram 2 weeks and 6 weeks post procedure
Secondary Ureteral Stricture Quality will be graded as either narrowed or obliterated segment. 2 weeks and 6 weeks post procedure
See also
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Recruiting NCT04441320 - Coated Metal Ureteral Stent in the Treatment of Radiation Induced Ureteral Stricture N/A
Recruiting NCT04129645 - Safety and Efficacy of URS Stents in the Treatment of Ureteral Stricture