Home monitoring of bladder pressure with a new device
Measurement of Bladder Pressure With a Novel External Device (Cystomanometer) - Home Use
This study is testing a new device that helps people with neurogenic bladder monitor their bladder pressure at home while using catheters to see if it works better than regular doctor visits.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 50 (estimated) |
| Ages | 1 Year to 99 Years |
| Sex | All |
| Sponsor | University of Iowa Academic / other |
| Locations | 1 site (Iowa City, Iowa) |
| Trial ID | NCT04128709 on ClinicalTrials.gov |
What this trial studies
This study evaluates a novel pressure monitoring device designed for patients with neurogenic bladder who use urinary catheters. The device attaches to standard catheters and allows for regular monitoring of bladder pressure and capacity in a home setting, which is crucial for maintaining renal and urinary health. Participants will use the device at least twice daily for two weeks, providing insights into its usability and effectiveness compared to traditional in-office testing.
Who should consider this trial
Good fit: Ideal candidates are patients diagnosed with neurogenic bladder who perform clean intermittent catheterization daily.
Not a fit: Patients who do not have a neurogenic bladder or do not use urinary catheters will not benefit from this study.
Why it matters
Potential benefit: If successful, this device could enable better management of bladder health for patients with neurogenic bladder, potentially preventing renal deterioration.
How similar studies have performed: Other studies have shown success with similar home monitoring approaches, indicating potential for this device to be effective.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * must have diagnosed neurogenic bladder Exclusion Criteria: * None
Where this trial is running
Iowa City, Iowa
- University of Iowa Hospital and Clinics — Iowa City, Iowa, United States (Recruiting)
Study contacts
- Principal investigator: Christopher S Cooper, MD — University of Iowa
- Study coordinator: Christopher S Cooper, MD
- Email: christopher-cooper@uiowa.edu
- Phone: 319-384-8922
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.