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OpenTrials
Completed

NCT Number: NCT05626686

An Exploratory Investigation of the Effects of Single Use vs. Reuse Catheters in Intermittent Catheterization

The overall aim of the investigation is to investigate the effect of repeated reuse of intermittent urinary catheters and to observe the impact of switch from single use to multiple reuse catheters.

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Key information

About this study

Throughout the investigation, the impact of switch from single use to multiple reuse catheters will be observed and compared with respect to health-related quality of life (HR-QoL), satisfaction, perception, and preference in female and male catheter-users, who use clean intermittent catheterization (CIC) for bladder management.

Furthermore, the investigation intends to identify microbial contamination of reused catheters and compare proportions to a control single use catheter.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • ≥18 years of age and has full legal capacity
  • Signed informed consent form
  • Use clean intermittent catheterization to the greatest extent possible (at least three times daily) for at least the last 1 month prior to inclusion
  • Ability (assessed by the investigator) and willingness to participate in a 4-week study period with at least three catheterizations a day using the investigational test product
  • Self-catheterize using a single use hydrophilic coated catheter for at least 1 month prior to inclusion

Exclusion criteria

  • Participation in any other clinical intervention study during this investigation
  • Previous participation in this investigation
  • Any known allergies towards ingredients in the investigational device
  • Symptoms of UTI at time of inclusion, as judged by the investigator
  • Antibiotic treatment within 2 weeks prior to the Baseline visit (V1)
  • Pregnancy
  • Breastfeeding

Treatment and study plan

CLINY catheter

Device

Subjects using a single use catheter for bladder management at inclusion. During the study period, subjects will use the reusable CLINY catheter for 28 test-days

Primary outcomes

  1. Change in Health-related Quality of Life From Baseline (Visit 1) to Termination (Visit 5), Measured by the Intermittent Self-Catheterization Questionnaire Index Score.

    Time frame: Baseline (day 0) and Termination (day 28).

    The Intermittent Self-Catheterization Questionnaire is a validated, self-reported questionnaire which is scored on a 5-point Likert scale and is translated to a value ranging from 0 (strongly disagree) to 4 (strongly agree) with higher values corresponding to greater Health-related Quality of Life. The aggregate scores across domains and the total score are calculated by averaging and multiplying by 25 to achieve a 100-point scale. Change = (Termination score - Baseline score)

Secondary outcomes

  1. Adverse Events

    Time frame: 28 days

    Number of Adverse Events during the study

Sponsors and collaborators

Lead sponsor

Coloplast A/S

Industry

Registry information

Important dates

Study start
2022
Primary completion
2023
Study completion
2023
First posted
Nov 25, 2022
Registry last updated
Apr 15, 2024

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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