CClinicalTrials.gg
Enrolling by invitationNCT07220980Updated Feb 27, 2026

Optimal Duration of Foley Catheter After Bulbar Urethroplasty

An interventional study of Early catheter removal and Later catheter removal in Urethral Stricture, Bulbar, sponsored by Jane Kurtzman. Enrolling by invitation at 4 sites in United States. Open to male participants aged 18 Years to 70 Years. Per ClinicalTrials.gov, last updated 2026-02-27.

Sponsored by Jane Kurtzman · Not applicable, Interventional, and Other

From the registry’s dates

  • Registered 1 year 1 month after the study started (first participant enrolled Aug 2024, registered Oct 2025).
Phase
Not applicable
Study type
Interventional
Enrollment
320
Allocation
Randomized
Ages
18 Years to 70 Years
Sex
Male
01

Study summary

The goal of this clinical trial is to learn when is the best time to remove a Foley catheter (tube used to drain urine from the bladder) after surgery in adult men who have a specific type of urethral stricture disease (narrowing of the tube that carries urine from the body). The main question it aims to answer is:

- Is there a difference between removing the catheter at 7-10 days versus 18-21 days?

Researchers will compare Foley removal at 7-10 days to removal at 18-21 days to see if there is a difference in problems after surgery or if the narrowing returns.

Participants will:

  • Complete a survey before surgery, when the catheter is removed, and within 12 months after surgery
  • Complete follow-up visits after surgery based on your specific medical needs and standard of care
02

Conditions studied

  • Urethral Stricture, Bulbar

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03

In context

Urethral Stricture

68 studies on the registry are indexed under Urethral Stricture; 23 are open to participants now.

This study's planned enrollment of 320 is above the median of 60 across 53 interventional studies indexed under Urethral Stricture.

Browse Urethral Stricture studies →

Lead sponsor

This is the only study on the registry with Jane Kurtzman as lead sponsor.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 70 Years
Sexes eligible
Male
Accepts healthy volunteers
No

Inclusion criteria

  • Cis-male patients
  • Age 18-70, inclusive
  • Bulbar urethral stricture undergoing a urethroplasty
  • Urethral stricture defect less than or equal to 7cm in length
  • First time urethroplasty
  • Negative urine analysis or urine culture

Exclusion criteria

Exclusion Criteria:

  • History of pelvic radiation
  • Diabetes with Hba1c greater than 8%
  • Penile urethral stricture
  • Posterior urethroplasty
  • Bulbar stricture greater than 7cm
05

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
320 participants (estimated)

Study arms

  • Experimental
    Early Removal

    Device: Early catheter removal

  • Experimental
    Later Removal

    Device: Later catheter removal

Interventions

  • DeviceEarly catheter removal

    Removal after 7-10 days

  • DeviceLater catheter removal

    Removal after 18-21 days

06

What researchers measure

Primary outcomes

  1. Number of Participants who Experience a Stricture Recurrence

    Time frame: 1 year

  2. Number of Participants who Experience a Perioperative Complication

    Time frame: From Foley insertion to Foley removal

Secondary outcomes

  1. Rate of Retrograde Urethrograms Performed on Day of Foley Removal

    Time frame: Foley Removal

07

Study locations

4 sites
  • Lahey Hospital & Medical Center
    Burlington, Massachusetts 01805, United States
  • Western New York Urology Associates
    Buffalo, New York 14203, United States
  • Ohio State University
    Columbus, Ohio 43212, United States
  • University of Utah Hospital
    Salt Lake City, Utah 84132, United States
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 27, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07220980
Lead sponsor
Jane Kurtzman
Collaborators
University of Minnesota
Responsible party
Jane Kurtzman (Assistant Professor, University of Utah) — Sponsor-investigator
First posted
Oct 27, 2025
Start date
Aug 28, 2024
Primary completion
Sep 2027 (estimated)
Completion
Sep 2027 (estimated)
Last update
Feb 27, 2026

Oversight

FDA-regulated drug
No
FDA-regulated device
Yes
View the source record on ClinicalTrials.gov ↗

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No contact was published for this record. The registry link below has the sponsor’s details.

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