Clinical Evaluation of Connected Catheter 2P (C2P) Wireless Urinary Prosthesis for Management of Neurogenic Lower Urinary Tract Dysfunction
Overview
- Phase
- N/A
- Intervention
- Not specified
- Conditions
- Urinary Retention
- Sponsor
- Spinal Singularity
- Enrollment
- 27
- Locations
- 8
- Primary Endpoint
- Freedom from genito-urinary injury/trauma
- Status
- Completed
- Last Updated
- 7 years ago
Overview
Brief Summary
The objective of this study is to evaluate the safety and essential performance of the C2P System in males with neurogenic lower urinary tract dysfunction (NLUTD), both in an acute clinical setting and an extended period of home use.
Detailed Description
Spinal Singularity had developed C2P system to address several drawbacks of current standard-of-care urinary catheters. The C2P is fully internal, urethral indwelling urinary prosthesis designed for improved bladder management in males with urinary retention disorders requiring catheterization, including NLUTD. The C2P is a sterile, single-extended use device that resides fully internally to the male lower urinary tract for an intended service life of up to 29 days per catheter
Investigators
Eligibility Criteria
Inclusion Criteria
- •Males age ≥ 18 with clinical diagnosis of neurogenic lower urinary tract dysfunction (NLUTD)
- •Must be clinically suitable and capable of safely managing bladder using an intermittent voiding or indwelling strategy
- •Must have stable urinary management history: no significant changes in bladder management regimen within past 12 months
- •Must have urodynamic profile suitable for C2P, as assessed via urodynamics study within past 12 months (including bladder capacity \> 200mL without uninhibited bladder contractions)
- •Subject's lower urinary tract anatomy must fall within the ranges serviceable by the C2P device, as specified in the investigational device instructions for use (IFU).
Exclusion Criteria
- •Active symptomatic urinary tract infection, as defined in this protocol (subjects may receive the device after Urinary Tract Infection (UTI) has been treated)
- •Significant risk profile or recent history of urethral stricture (e.g. stricture within past 90 days)
- •Significant risk profile or recent history of clinically significant autonomic dysreflexia (AD) (e.g. History of hospitalization due to AD within past 12 months)
- •Significant intermittent urinary incontinence (between catheterizations)
- •Uninhibited bladder contractions and/or vesico-ureteral reflux that is not reliably controlled with medication or alternate therapy (e.g. Botox injections)
- •Pre-existing urinary pathologies and/or morphological abnormalities of the lower urinary tract or bladder (assessed during in-depth medical screening, including cystoscopy and urine analysis)
- •Urinary tract inflammation or neoplasm
- •Urinary fistula
- •Bladder diverticulum (outpouching) \> 5cm in size
- •Chronic pyelonephritis (secondary to upper urinary tract infection(s) within past 6 months)
Outcomes
Primary Outcomes
Freedom from genito-urinary injury/trauma
Time Frame: 3 months
Improved bladder management without injury to genito-urinary tract
Successful Home-use Performance
Time Frame: 3 months
To evaluate successful home use of C2P using same measures as Acute Performance
Successful Acute Performance- I
Time Frame: Day 0 (On the day of C2P insertion)
To evaluate successful retention of C2P
Successful Acute Performance- II
Time Frame: Day 0 (On the day of C2P insertion)
To evaluate successful bladder voiding with C2P
Successful Acute Performance- III
Time Frame: Day 0 (On the day of C2P insertion)
To evaluate successful valve sealing of C2P