Actively Recruiting

Age: 18Years +
All Genders
ID06384079

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

Led by Northwestern University · Updated on 2024-11-26

25

Participants Needed

1

Research Sites

260 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are studying how the length of ureteral rest—the time between changing a ureteral stent to a percutaneous nephrostomy tube—affects the length of ureteral strictures before surgery to repair the ureter. The study focuses on patients with ureteral strictures who are preparing for ureteral reconstruction surgery. The goal is to better understand this timing to potentially improve surgical outcomes. Participants will undergo antegrade and retrograde pyelogram procedures before their ureteral repair surgery. These imaging tests are used to measure the ureteral stricture length and quality at two time points: 2 weeks and 6 weeks after the procedure. The study is observational, and all participants will receive these imaging evaluations as part of the research. During the study, participants will be monitored through these imaging assessments to evaluate the stricture length and whether the narrowed segment is classified as narrowed or obliterated. The study will review these measurements to assess the effect of ureteral rest duration. Participation involves signing informed consent and completing the imaging procedures, with no additional treatments or interventions required. The study is expected to continue until November 2030.

CONDITIONS

Brief Title

Duration of Ureteral Rest Prior to Ureteral Reconstruction Surgery

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Over 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
Not Eligible

You will not qualify if you...

  • Under 18 years of age
  • Unable to provide informed consent
  • Members of vulnerable patient populations

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Diagnostic Evaluation

Duration - 1 day

Participants undergo antegrade and retrograde pyelogram procedures prior to ureteral reconstruction surgery to assess ureteral stricture length and quality.

1 visit (in-person)

Long-term Monitoring

Duration - 6 weeks

Participants are monitored after the diagnostic procedures to evaluate ureteral stricture length and quality at 2 weeks and 6 weeks post procedure.

2 visits (in-person) at 2 weeks and 6 weeks post procedure

Trial Site Locations

Total: 1 location

1

Northwestern University

Chicago, Illinois, United States, 60611

Actively Recruiting

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Research Team

E

Emily Ji

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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