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NCT03447639 · ClinicalTrials.gov registry record · Phase 4

Betadine Bladder Irrigations vs. Standard of Care Prior to Indwelling Catheter Removal

A Phase 4 study, sponsored by Corewell Health East.

Terminated
Registry status
Phase 4
Development phase
3
Enrollment target

NCT03447639: Clinical Trial Phase 4 study, sponsored by Corewell Health East.

NCT03447639 is a Phase 4 study that was terminated before completion, run by Corewell Health East. The registered enrollment target is 3 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (99% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03447639, a Phase 4 study, was terminated before completion, sponsored by Corewell Health East.

TERMINATED
Registry status
Phase 4
Development phase
3 participants
Enrollment target

Study Summary

Over the last decade, there has been great emphasis on reducing the incidence of hospital-acquired infections, including catheter-associated UTI (CAUTI). This study will evaluate the effectiveness of Betadine irrigation solution (2% povidone-iodine) instilled into the bladder immediately prior to indwelling catheter removal to decrease the risk of subsequent bacteriuria, leading to decreased rates of NHSN defined CAUTI.

Primary Outcome

Per NHSN defined catheter associated UTI (CAUTI) criteria

Interventions

  • DRUG Povidone-iodine irrigation

Trial Details

FieldValue
Enrollment Target 3 participants
Start Date 2018-03-29
Est. Completion 2018-10-22
Phase Phase 4
Corewell Health East

106 total trials

Why NCT03447639 stopped before completion

NCT03447639 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 3 participants, a relatively small participant target, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (99% lower).

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

NCT03447639 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03447639 about?

NCT03447639 is a clinical study titled "Betadine Bladder Irrigations vs. Standard of Care Prior to Indwelling Catheter Removal". Over the last decade, there has been great emphasis on reducing the incidence of hospital-acquired infections, including catheter-associated UTI (CAUTI). This study will evaluate the effectiveness of Betadine irrigation solution (2% povidone-iodine) instilled into the bladder immediately prior to in...

What is the current status of trial NCT03447639?

This trial is currently terminated. It is a Phase 4 study. The enrollment target is 3 participants. The study started on 2018-03-29. Estimated completion is 2018-10-22.

What interventions are being tested in trial NCT03447639?

The interventions under investigation include: Povidone-iodine irrigation (DRUG).

Who is sponsoring clinical trial NCT03447639?

This trial is sponsored by Corewell Health East, which has 106 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03447639's enrollment target sits among peer trials

3 1995th of 2000 higher than 3 of 2,000 other Phase 4 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 4 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 NCT03447639, the US trial registry maintained by the National Library of Medicine. NCT03447639 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.