Status:

TERMINATED

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

Lead Sponsor:

Corewell Health East

Conditions:

Catheter; Infection (Indwelling Catheter)

Catheter Infection

Eligibility:

MALE

18+ years

Phase:

PHASE4

Brief 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 ...

Detailed Description

Indwelling urinary catheters are routinely used in the care of hospitalized patients for a variety of reasons, including monitoring of urine output in critically ill patients, relief of urinary obstru...

Eligibility Criteria

Inclusion

  • Provide written informed consent and the willingness and ability to comply with all aspects of study requirements
  • Male
  • Inpatients ≥ 18 years of age with an indwelling catheter in place for at least 5 days with a plan for removal

Exclusion

  • Patients planned for discharge with an indwelling catheter in place
  • Patients unable to report urinary symptoms accurately
  • Patients with hyper-sensitivity or allergic reaction to Betadine, iodine, shellfish or other related compounds
  • Clinical signs or symptoms of urinary tract infection at the time of consent
  • Patients currently being treated for UTI
  • Patients currently taking any antibiotic medication, other than vancomycin, linezolid, daptomycin, clindamycin, or metronidazole.
  • Patients already taking medications known to potentially irritate the bladder, such as, but not limited to, cyclophosphamide, ifosfamide, and other chemotherapeutic agents
  • Patients with history of bladder cancer, pelvic radiation or interstitial cystitis
  • Patients unable to comply with study requirements
  • Any other condition which, per investigators' judgment, may increase patient risk and/or impede the reliability of study data

Key Trial Info

Start Date :

March 29 2018

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

October 22 2018

Estimated Enrollment :

3 Patients enrolled

Trial Details

Trial ID

NCT03447639

Start Date

March 29 2018

End Date

October 22 2018

Last Update

January 18 2020

Active Locations (1)

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Beaumont Hospital

Royal Oak, Michigan, United States, 48073