Comparison of Urinary Flow Study (NCT06918067)
Comparison of Urinary Flow Speed Using 14 Fr Two Eyelet Coloplast Female SpeediCath Urinary Catheter Versus 14 Fr Coloplast Micro Zone Luja Female Catheter in Female Patients Using Intermittent Catheters
🩺 Plain-English Summary (8th-Grade Level)
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.
Who can join: Review the eligibility criteria below.
Location: Women's Center for Pelvic Health (Mercy) — Charlotte, North Carolina
Age range: 18 Years
🧪 Interventions in This Study
📋 "Do I Qualify?" — 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria ↗
📍 All Participating Trial Locations (1 Sites)
- Women's Center for Pelvic Health (Mercy) — Charlotte, North Carolina
📞 Contact the Study Coordinator
Phone: (704) 304-1160
Email: michael.kennelly@atriumhealth.org
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
💰 Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA § 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
More studies in Urinary Retention
- How the Method of Bladder Emptying After Epidural Placement in Labor Affects Postpartum Voiding — Pittsburgh, Pennsylvania
- Consumer Evaluation of an Investigational Intermittent Catheter — Libertyville, Illinois
- Post-operative Urinary Retention (POUR) Following Thoracic Surgery — Hackensack, New Jersey
- Rectus Abdominis Detrusor Myoplasty for Urinary Retention — Cleveland, Ohio
- Post Operative Urinary Retention (POUR) Following Thoracic Oncological Surgery — Brick, New Jersey
Explore by condition: All Urinary Retention clinical trials
💡 How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.