Status:
COMPLETED
BlueWind Medical System for the Treatment of Patients With OAB
Lead Sponsor:
BlueWind Medical
Conditions:
Over Active Bladder
Eligibility:
All Genders
18-80 years
Phase:
NA
Brief Summary
BlueWind system safety and performance in treatment of patients diagnosed with overactive bladder (OAB)
Detailed Description
BlueWind Medical system safety and performance in treatment of patients diagnosed with overactive bladder (OAB)
Eligibility Criteria
Inclusion
- Signed written informed consent.
- Male or female aged 18 - 80.
- Patient agrees to attend all follow-up evaluations and is willing to completely and accurately fill out voiding diaries and questionnaires, and is willing to complete required exams and tests.
- Patients with overactive bladder symptoms:
- Urinary frequency greater than 8 times/24 hours AND/OR Urinary urgency leaks of at least 2 leaks on 3 day voiding diary
- Patient who has failed conservative treatment after at least 6 months of treatment
- Patients with normally functioning upper urinary tract.
- Patients with no clinical evidence of a neurological S2-S4 motor sensory deficit.
- Prior PTNS Group: Patients who have had successful PTNS treatment (successful treatment is defined as ≥50% reduction in urinary frequency, and/or ≥50% fewer incontinence episodes, or a return to normal voiding frequency \[\<8 voids/day\], based on retrospective diary review).
- De novo Patient Group: Patient who passes the BlueWind compatibility test.
Exclusion
- Any metal implant in the area of BlueWind Medical implantation site.
- Patients who have not had stable OAB medications for at least 30 days.
- Patients who have received botulinum toxin injections within the past 6 months.
- Previous urinary incontinence surgery or implantation of artificial graft material within the last 6 months.
- Any spinal or genitourinary surgery within the last 6 months. Pelvic pain disorders
- Obvious clinically demonstrated genuine stress incontinence.
- Any neurological disease or disorder including neuropathy or injury resulting in neuropathy.
- Current urinary tract infection, presence of urinary stone and/or urinary tract malignancy (i.e. tumor, vesicourethral reflux, etc.)
- Pelvic radiotherapy and chemotherapy.
- Severe uncontrolled diabetes.
- Patients anticipating magnetic resonance imaging (MRI) exams.
- Presence of cystocele, enterocele or rectocele of grade 3 or 4.
- Prior PTNS Group: Patients who are receiving concomitant nerve stimulation therapies for OAB treatment, except for PTNS maintenance therapy.
- De novo Patient Group: Patients who have received or are receiving nerve stimulation therapies for OAB treatment, including PTNS.
Key Trial Info
Start Date :
February 1 2015
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
December 1 2018
Estimated Enrollment :
36 Patients enrolled
Trial Details
Trial ID
NCT02299544
Start Date
February 1 2015
End Date
December 1 2018
Last Update
June 18 2019
Active Locations (6)
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1
Catharina Ziekenhuis
Eindhoven, Netherlands
2
Maastricht UMC
Maastricht, Netherlands
3
Radboud university medical center Department of Urology
Nijmegen, Netherlands
4
Southmead Hosital
Bristol, United Kingdom