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Duration of Ureteral Rest Prior to Ureteral Reconstruction Surgery

Study to Assess Duration of Ureteral Rest Prior to Ureteral Reconstruction Surgery

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06384079
Enrollment
25
Registered
2024-04-25
Start date
2024-09-24
Completion date
2030-11-30
Last updated
2024-11-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Ureteral Stricture

Brief 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.

Interventions

PROCEDUREAntegrade and retrograde pyelogram

Participation in the study will guarantee that participants will receive this procedure.

Sponsors

Northwestern University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frame
Ureteral stricture length measured by antegrade or retrograde pyelogram2 weeks and 6 weeks post procedure

Secondary

MeasureTime frame
Ureteral Stricture Quality will be graded as either narrowed or obliterated segment.2 weeks and 6 weeks post procedure

Countries

United States

Contacts

Primary ContactEmily Ji
emily.ji@nm.org312-695-8146

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026