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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 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.
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
| Field | Value |
|---|---|
| Enrollment Target | 25 participants |
| Start Date | 2024-09-24 |
| Est. Completion | 2030-11 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06384079
The ClinicalTrials.gov registry entry for NCT06384079 describes a study currently listed as recruiting, categorized as an unspecified phase. The registered enrollment target is 25 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Northwestern University, which has 1,209 total studies on file at ClinicalTrials.gov.
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 1 study location spanning 1 distinct geographic area - top geographies include 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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