ClinicalTrials.gg
Not yet recruitingNCT07930468Updated Nov 12, 2026

Optimal Duration of Urinary Catheterization After Right-Sided Colectomy

An interventional study of Immediate Urinary Catheter Removal and Postoperative Day 1 Urinary Catheter Removal in Post Operative Urinary Retention, Urinary Retention After Procedure and Urinary Retention Postoperative, sponsored by University of Southern California. Not yet recruiting at 2 sites in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-11-12.

Sponsored by University of Southern California · Not applicable, Interventional, and Supportive care

Updated Nov 12, 2026Newly registeredGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
190
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Where this study stands

Counted across the records on this site · 2026-11-13

Among 272 studies in Urinary Tract Infections with a site in United States — 44 open to participants now, 54 under way, 2 of them phase 3. Urinary Tract Infections · United States.

Planned enrollment
79th of 223
190 · median 100
Started
2026
with 17 others
No phase
93 of 272
20 open now
Primary completion
2028-05
later than 41 of 53 live
Registered
272nd of 272
by date

Among the 272 studies in Urinary Tract Infections with a site in United States, this one is the 79th largest by planned enrollment of the 223 interventional ones that give a count, is one of 18 that started in 2026, is one of 93 with no phase, reaches primary completion later than 41 of the 53 other live ones, and was the 272nd registered.

Urinary Tract Infections

804 studies on the registry are indexed under Urinary Tract Infections; 133 are open to participants now.

Browse Urinary Tract Infections studies →

Open to participants now

44 of the 272 studies in Urinary Tract Infections with a site in United States are open now. Recruiting first, the newest first:

39 more — sign in →

All 44 open studies →

A study can be open while its sites in United States have not opened yet or have stopped. Only those recruiting at a site in United States →

Who these studies take

Of the 84 Urinary Tract Infections studies recruiting now, 50 (60%) set no upper age limit and 23 (27%) stop at 75 or younger; 15 take children under 18; 17 take healthy volunteers.

This study: 18 Years and older · all sexes · no healthy volunteers.

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02

Study summary

The goal of this prospective, randomized trial is to determine the optimal duration of urinary catheterization in patients that receive elective, right-sided colectomy. The main objectives of this study are:

  • To compare rates of urinary retention in patients with post operative urinary catheter duration of 0 days and 1 day following right-sided colectomy.
  • To compare rates of urinary tract infection (UTI) in patients with postoperative urinary catheter duration of 0 days and 1 day following right-sided colectomy.

Enrolled participants will be randomized to one of two groups, immediate removal of urinary catheter at the conclusion of the operation or removal of urinary catheter on post operative day one.

Read the detailed description

Urinary catheterization is indicated for various operations conducted by colorectal surgeons. This process allows a tube to be inserted into the bladder to provide decompression while the patient is anesthetized. Prolonged urinary catheter placement is associated with urinary retention, urinary tract infections, and increased hospital length of stay. Clinical guidelines recommend urinary catheter discontinuation within 24 hours of operation but there is mixed evidence to support this recommendation. Further, there is a paucity of data that investigates optimal urinary catheter duration in specific colorectal surgery operations.

This prospective, randomized clinical trial aims to identify the optimal urinary catheter duration for patients undergoing elective, right-sided colectomy. Patients will be randomized into two groups: 1) urinary catheter discontinuation at the completion of surgery, or 2) urinary catheter discontinuation on post operative day 1. The primary objective is to compare rates of urinary retention between groups. The investigators hypothesize that patients with immediate urinary catheter discontinuation will have reduced rates of urinary retention and urinary tract infections compared to the group with urinary catheters maintained until post operative day 1.

03

Conditions studied

  • Post Operative Urinary Retention
  • Urinary Retention After Procedure
  • Urinary Retention Postoperative
  • Urinary Tract Infection (Diagnosis)

Keywords

  • urinary catheter
  • Foley catheter
  • catheter removal
  • right hemicolectomy
  • right-sided colectomy
  • ileocecectomy
  • enhanced recovery after surgery
  • ERAS
  • noninferiority
04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Age 18 years or older.
  • Scheduled for elective ileocecectomy, right hemicolectomy, or extended right hemicolectomy using an open, laparoscopic, or robotic approach.
  • physical status class I-III.
  • Ability and willingness to provide written .

Exclusion criteria

Exclusion Criteria:

  • History of urinary tract .
  • Emergent or urgent surgery.
  • Right hemicolectomy performed with another major surgical procedure on the same day.
  • Genitourinary tract injury during surgery that precludes participation.
  • History of urinary retention following a previous procedure, surgery, or urinary catheter removal.
  • History of urinary retention that is not being actively treated.
  • Neurogenic bladder.
  • Chronic indwelling Foley catheter or suprapubic catheter.
  • History of cystectomy or a surgically created urinary conduit, including a neobladder or ileal conduit.
  • Chronic kidney disease greater than stage 2.
  • History of chronic urinary tract infection.
  • Current extravesicular or enterourethral fistula.
  • Perioperative epidural catheter placement.
  • Incarceration.
  • Inability or unwillingness to provide .
  • Pregnancy.
Terms in these criteria, in plain language(3)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

ASA physical status

The anaesthetists’ scale of health before surgery: I is healthy, II has a mild illness that is under control, III a severe one, IV a severe illness that is a constant threat to life. V and VI are used for the critically ill and for organ donors.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

Cancer (malignancy)

Malignancy means cancer. Criteria about another or earlier malignancy ask whether you have had a different cancer, usually within a set number of years.

Some are commonly allowed, such as treated skin cancers other than melanoma and early cancers removed completely — check the exceptions this study lists.

05

Study design

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

Study arms

  • Experimental
    Immediate Catheter Removal

    Participants will undergo urinary catheter removal immediately after completion of surgery, in the operating room on post operative day 0.

    Procedure: Immediate Urinary Catheter Removal

  • Active comparator
    Postoperative Day 1 Catheter Removal

    Participants will undergo urinary catheter removal on post operative day 1.

    Procedure: Postoperative Day 1 Urinary Catheter Removal

Interventions

  • ProcedureImmediate Urinary Catheter Removal

    Removal of the urinary catheter immediately after elective right hemicolectomy before leaving the operating room.

    Also known as: POD0 catheter removal, Immediate Foley Removal

  • ProcedurePostoperative Day 1 Urinary Catheter Removal

    Removal of the intra-operatively placed Foley urinary catheter on the day after elective right-sided colectomy, post-operative day one.

    Also known as: removal POD1 catheter removal, next-day Foley removal

06

What researchers measure

Primary outcomes

  1. Percentage of Participants With Post Operative Urinary Retention

    Post operative urinary retention will be identified by inability to void within 8 hours after catheter removal, associated suprapubic fullness and/or tenderness, and a bladder scan volume greater than 300 mL; or by spontaneous voiding with urinary symptoms and a post-void residual volume greater than 300 mL. Symptoms include suprapubic pain or fullness, bladder pressure, incomplete emptying, or straining.

    Time frame: From initial post operative urinary catheter removal through hospital discharge, assessed up to 90 days.

Secondary outcomes

  1. Percentage of Participants With Urinary Tract Infection

    Urinary tract infection will be identified by clinical signs or symptoms such as suprapubic pain or tenderness, dysuria, hematuria, or urinary frequency, together with a urine culture showing more than 100,000 colony-forming units/mL of bacteria. Urinalysis and urine culture will be obtained only when infection is clinically suspected.

    Time frame: From post operative day one through hospital discharge, assessed up to 90 days.

  2. Postoperative Hospital Length of Stay

    Number of inpatient hospital days from the day of surgery to the day of discharge.

    Time frame: From post operative day one through hospital discharge, assessed up to 90 days.

07

Study locations

2 sites
08

References and documents

Individual participant data

Plan to share: No — Consent does not permit sharing; will revisit

No publications or documents are linked to this record.

09

Timeline

1 registry update since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Start is estimated for Nov 2026; primary completion for May 2028, 18 months later.

Of 136 non-industry interventional studies with no phase under Urinary Tract Infections, half reached primary completion within 23 months of starting (the median), counting those still running; a quarter within 8 and three quarters within 39. This study's planned 18 months is below that.

Counting every sponsor, half of 153 studies reached it within 22 months; a quarter within 8 and three quarters within 37.

How these figures are worked out, and which studies are left out of them.

Registered
Nov 2, 2026
First posted
Nov 12, 2026
StartEst.
Nov 30, 2026
Primary completionEst.
May 30, 2028
CompletionEst.
Nov 30, 2028
Last update
Nov 12, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
Registered
First appeared on the registry. No changes since
Nov 12, 2026
Show all 1 update
  1. Nov 12, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07930468
Responsible party
Sacha Broccard (Faculty Physician, USC Keck, University of Southern California) — Principal investigator
First posted
Nov 12, 2026
Start date
Nov 30, 2026 (estimated)
Primary completion
May 30, 2028 (estimated)
Completion
Nov 30, 2028 (estimated)
Last update
Nov 12, 2026

Study contacts

Sacha Broccard, MD
Contact
Sacha.Broccard@med.usc.edu
201-675-8256

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Nov 2026. You cannot join it, but the record below documents what was studied.

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