ClinicalTrials.Veeva

Menu

Duration of Ureteral Rest Prior to Ureteral Reconstruction Surgery

Northwestern University logo

Northwestern University

Status

Enrolling

Conditions

Ureteral Stricture

Treatments

Procedure: Antegrade and retrograde pyelogram

Study type

Observational

Funder types

Other

Identifiers

NCT06384079
STU00219828

Details and patient eligibility

About

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.

Enrollment

25 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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

Trial design

25 participants in 1 patient group

Endoscopic Evaluation
Description:
Antegrade and retrograde pyelogram will be completed prior to definitive ureteral repair
Treatment:
Procedure: Antegrade and retrograde pyelogram

Trial documents
1

Trial contacts and locations

1

Loading...

Central trial contact

Emily Ji

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems