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NCT02247960 · ClinicalTrials.gov registry record · NA

Antibiotic Prophylaxis for Urinary Catheter Removal After Radical Prostatectomy

A NA study, sponsored by University of Rochester.

Terminated
Registry status
NA
Development phase
175
Enrollment target

NCT02247960: Clinical Trial NA study, sponsored by University of Rochester.

NCT02247960 is a NA study that was terminated before completion, run by University of Rochester. The registered enrollment target is 175 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (88% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02247960, a NA study, was terminated before completion, sponsored by University of Rochester.

TERMINATED
Registry status
NA
Development phase
175 participants
Enrollment target

Study Summary

The aim of this study is to determine whether antibiotics prophylaxis at the time of urinary catheter removal decreases the number of symptomatic urinary tract infections in patients after radical prostatectomy. In addition, the investigators aim to determine whether antibiotic prophylaxis is potentially harmful to patients (e.g. adverse reactions from antibiotic use, resistant bacteria in the urine, Clostridium difficile infections etc.). The investigators also aim to identify specific populations that may be at higher risk of developing urinary tract infections with urinary catheter use after radical prostatectomy.

Primary Outcome

After removal of the catheter, urine was tested for infection whenever symptoms were experienced by the participants from the time they enrolled to 12 months following their operation.

Interventions

  • DRUG Ciprofloxacin

Trial Details

FieldValue
Enrollment Target 175 participants
Start Date 2014-07
Est. Completion 2016-05
Phase NA
University of Rochester

636 total trials

Why NCT02247960 stopped before completion

NCT02247960 is an interventional study that assigns participants to a tested intervention. The registered 175 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (88% lower).

The record links to 0 conditions, and to 1 intervention - of which Ciprofloxacin is the first listed.

NCT02247960 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02247960 about?

NCT02247960 is a clinical study titled "Antibiotic Prophylaxis for Urinary Catheter Removal After Radical Prostatectomy". The aim of this study is to determine whether antibiotics prophylaxis at the time of urinary catheter removal decreases the number of symptomatic urinary tract infections in patients after radical prostatectomy. In addition, the investigators aim to determine whether antibiotic prophylaxis is potent...

What is the current status of trial NCT02247960?

This trial is currently terminated. It is a NA study. The enrollment target is 175 participants. The study started on 2014-07. Estimated completion is 2016-05.

What interventions are being tested in trial NCT02247960?

The interventions under investigation include: Ciprofloxacin (DRUG).

Who is sponsoring clinical trial NCT02247960?

This trial is sponsored by University of Rochester, which has 636 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02247960's enrollment target sits among peer trials

175 610th of 2000 higher than 1,391 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT02247960, the US trial registry maintained by the National Library of Medicine. NCT02247960 (mid enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.