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Recruiting NCT06918067

Comparison of Urinary Flow Study

Trial Parameters

Condition Urinary Retention
Sponsor Wake Forest University Health Sciences
Study Type INTERVENTIONAL
Phase N/A
Enrollment 17
Sex FEMALE
Min Age 18 Years
Max Age N/A
Start Date 2025-11-06
Completion 2027-03
Interventions
Coloplast Micro Zone Luja Female CatheterColoplast SpeediCath Female Catheter

Brief Summary

The purpose of this research study is to compare the urinary flow speed of two different female catheters in patients that use intermittent catheters to empty their bladder. The "14 Fr Two Eyelet Coloplast Female SpeediCath Urinary Catheter" will be compared to the "14 Fr Coloplast Micro Zone Luja Female Catheter." Participants will have one study visit that should take about an hour and will also receive a follow-up telephone call about one week after the visit.

Eligibility Criteria

Inclusion Criteria: * Female * Regular use of intermittent catheters to empty bladder, for at least 1 month before enrolment * Age 18 years or older * Required to adhere to the intervention procedure and not participate in any other clinical studies throughout the duration of this study Exclusion Criteria: * Severe urinary tract abnormalities (e.g. excessive production of urinary mucus/sediments/debris) * Hypersensitive to the ingredients in the catheters being tested * Recent surgery, within 3 months * Currently being treated for urinary tract infection * Being pregnant or breastfeeding * Non-English speaking

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