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NCT06384079 · ClinicalTrials.gov registry record

Duration of Ureteral Rest Prior to Ureteral Reconstruction Surgery

A clinical trial of Ureteral Stricture, sponsored by Northwestern University.

Recruiting
Registry status
25
Enrollment target
1
Study location

NCT06384079: Recruiting study of Ureteral Stricture, sponsored by Northwestern University.

NCT06384079 is a study of Ureteral Stricture that is actively recruiting participants, run by Northwestern University. The registered enrollment target is 25 participants. The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06384079, a study of Ureteral Stricture, is actively recruiting participants, sponsored by Northwestern University.

RECRUITING
Registry status
25 participants
Enrollment target
1
Study location

Study 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.

Conditions Studied

Interventions

  • PROCEDURE Antegrade and retrograde pyelogram

Study Locations (1)

Illinois

  • Northwestern University - Chicago

Trial Details

FieldValue
Enrollment Target 25 participants
Start Date 2024-09-24
Est. Completion 2030-11
Northwestern University

1,209 total trials

What NCT06384079 shows while recruiting

NCT06384079 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 25 participants, a relatively small participant target.

The record links to 1 condition, with Ureteral Stricture appearing as the primary indexed condition, and to 1 intervention - of which Antegrade and retrograde pyelogram is the first listed.

NCT06384079 reports a single indexed study location in Illinois.

Frequently Asked Questions

What is clinical trial NCT06384079 about?

NCT06384079 is a clinical study titled "Duration of Ureteral Rest Prior to Ureteral Reconstruction Surgery". 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.

What is the current status of trial NCT06384079?

This trial is currently recruiting. The enrollment target is 25 participants. The study started on 2024-09-24. Estimated completion is 2030-11.

What conditions does trial NCT06384079 study?

This clinical trial studies the following conditions: Ureteral Stricture.

What interventions are being tested in trial NCT06384079?

The interventions under investigation include: Antegrade and retrograde pyelogram (PROCEDURE).

Who is sponsoring clinical trial NCT06384079?

This trial is sponsored by Northwestern University, which has 1,209 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06384079 being conducted?

This trial has 1 study location across Illinois. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Source: ClinicalTrials.gov NCT06384079, the US trial registry maintained by the National Library of Medicine. NCT06384079 (small enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.