Ureteral Stricture Clinical Trial
Official title:
Study to Assess Duration of Ureteral Rest Prior to Ureteral Reconstruction Surgery
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 |
Verified date | April 2024 |
Source | Northwestern University |
Contact | Emily Ji |
Phone | 312-695-8146 |
emily.ji[@]nm.org | |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
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.
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 |
Country | Name | City | State |
---|---|---|---|
United States | Northwestern University | Chicago | Illinois |
Lead Sponsor | Collaborator |
---|---|
Northwestern University |
United States,
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 |
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