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Enrolling by Invitation

NCT Number: NCT05775614

UROtainer for Bladder Catheter Maintenance, Infection Prevention and Quality of Life

The purpose of the current study is to investigate whether catheter flushing with Uro-Tainer® with citric acid and Uro-Tainer® Polihexanide can: Reduce catheter changes due to incrustation and blockage.

In addition, a list of secondary aims inclusive of cost-effectiveness analysis in collaboration with the Centre for Innovative Medical Technology (CIMT) at OUH.

Enrolling by Invitation

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Key information

Conditions

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Odense University Hospital

Odense, 5000, Denmark

About this study

The purpose of the current study is to investigate whether catheter flushing with Uro-Tainer® with citric acid and Uro-Tainer® Polihexanide can: Reduce catheter changes due to incrustation and blockage.

In addition, a list of secondary aims inclusive of cost-effectiveness analysis in collaboration with the Centre for Innovative Medical Technology (CIMT) at OUH.

There is a need for a randomised study to justify if Uro-Tainer® flushing will have an advantage over the cheaper and normally used Saline flushing.

Standard therapies vary depending on the blockage type and severity. Saline Solution can be used daily for a shorter period and 1-2 times a week for long-term catheter maintenance.

Study:

  • Uro-Tainer® Polihexanide two weekly rinses compared to two weekly rinses with saline for 3 months.
  • Uro-Tainer® with citric acid: Two weekly rinses compared to two weekly rinses with saline for 3 months.

Clinical benefits:

  • Less catheter blockage -> less need for catheter replacement outside the regular schedule -> Fewer infections and better QoL
  • It is expected that cost-effectiveness analysis will show a better economic outcome for the society
  • No unknown adverse effects are expected
  • The risk of participation in this study is very small compared to the expected effect of fewer catheter replacements, fewer infections and better QoL which justifies the selection of clinical endpoints.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Citizen not previously flushed

  • A permanent catheter (suprapubic and urethral)
  • Male and female > 18 years of age
  • Acute or previous catheter stop because of blocking or incrustations.
  • The pilot project does not include clogging due to incrustations
  • Voluntary consent to participate in the study, following a full explanation of the nature and purpose of the study, by signing the informed consent form approved by the Ethics Committee (EC) before all evaluations.

Citizen previously flushed with NaCl or UroTainer®

  • A permanent catheter (suprapubic and urethral)
  • Male and female > 18 years of age
  • Willingness to take a rinse break for a minimum of 4 weeks. In the event of 2 catheter stops during the flushing break, assessed on the basis of an urgent need for catheter flushing with NaCl or catheter change, the citizen can be included.
  • The pilot project does not include clogging due to incrustations
  • If there is no catheter stop during the rinsing break, the citizen will continue without rinsing until a possible catheter stop.
  • Voluntary consent to participate in the study, following a full explanation of the nature and purpose of the study, by signing the informed consent form approved by the Ethics Committee (EC) before all evaluations.

Exclusion criteria

  • Urothelial cancer
  • Bladder and kidney stones requiring treatment
  • Age < 18 years of age
  • Pregnant and / or breastfeeding women
  • Not able to understand Danish
  • Dementia, where relatives can / will not give consent
  • Simultaneous participation in another interventional clinical trial (drugs or medical devices studies)

Treatment and study plan

UroTainer®

Device

Clinical effect of preventive treatment - catheter flushing with UroTainer®

Saline

Device

Clinical effect of preventive treatment - catheter flushing with saline solution

Primary outcomes

  1. Number of catheter changes during the treatment and follow-up period.

    Time frame: 1 year

    Number of catheter changes

Secondary outcomes

  1. UTI events (Urinary tract infection event)

    Time frame: 1 year

    The number of prescriptions

  2. Urine culture

    Time frame: 1 year

    Urine culture performed if UTI is suspected

  3. Odour

    Time frame: 1 year

    Odour nuisance is to be assessed on a 5-point scale. A high score is a worse outcome.

    • No odour
    • Discreet odour nuisance after catheter care
    • Odour that is noticed once in a while. Noticed by the participant and relatives
    • Odour that is present all the time around the participant
    • Solid odour that is felt in all rooms. "It hangs" on the participant
  4. Quality of life by SF-36

    Time frame: 1 year

    SF-36 (Health Survey Short Form 36)

    The SF-36 consists of 36 items - that are grouped into 8 subscales or domains:

    Physical functioning (10 items); Role limitations due to physical health (4 items); Role limitations due to emotional problems (4 items); Energy/fatigue; Emotional well-being; Social functioning (2 items); Pain (2 items); General health. Aggregate scores for each domain range from 0 to 100, compiled as a percentage - where the higher the score, the more favourable the health state.

  5. Quality of life by ICIQ-LTCqol

    Time frame: 1 year

    Living with a long term catheter (ICIQ-LTCqol 12/12 ) The questionnaire consists of three scales yielding two summary measures catheter function and concern score, lifestyle impact and unscored items. Possible scores range from 1 to 530, with lower scores representing better catheter function, concern score and life impact.

  6. Cost effectiveness analyses 1

    Time frame: 1 year

    Costs of used catheters in DDK pr participant

  7. Cost effectiveness analyses 2

    Time frame: 1 year

    Costs of used solutions for the maintenance of indwelling urethral and suprapubic catheters in DKK pr participant

  8. Cost effectiveness analyses 3

    Time frame: 1 year

    Costs of used time of the health care professionals used for catheter maintenance and control in primary care in DKK pr participant

Sponsors and collaborators

Lead sponsor

Odense University Hospital

Other

Registry information

Official study title

Study of Uro-Tainer® Polihexanide and Uro-Tainer® With Citric Acid on Catheter Blockage, Infection Prevention, Cost-effectiveness and Quality of Life (UROBIQ): a Prospective Randomized Single-blinded Clinical Study

Acronym: UROBIQ

Important dates

Study start
2022
Primary completion
2027
Study completion
2028
First posted
Mar 20, 2023
Registry last updated
Sep 18, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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