This study evaluates the safety and efficacy of use of the Butterfly Medical's prostatic retraction device in Benign Prostatic Hyperplasia (BPH) Patients. The study follows patients implanted with the Butterfly device for up to 1 year after implantation. Evaluations include recording of safety events and BPH related symptoms by Uroflowmetry tests and International Prostate Symptom Score (IPSS) questionnaires. The study also assess sexual quality of life after implantation of the Butterfly device.
Benign prostatic hyperplasia (BPH) is a non-cancerous enlargement of the prostate gland that may restrict the flow of urine from the bladder. BPH is a cellular proliferative process of the prostate, also referred as enlarged prostate. An estimated 50% of men demonstrate histopathologic BPH by age 60 years. This number increases to 90% by age 85 years; thus, increasing gland size is considered a normal part of the aging process. Approximately half of those diagnosed with histopathologic BPH demonstrate moderate-to-severe BPH related symptoms (also known as Lower Urinary Tract Symptoms = LUTS), including urinary frequency, urgency, nocturia (getting up at night during sleep to urinate), decreased or intermittent force of stream, or a sensation of incomplete emptying. Complications occur less commonly but may include acute urinary retention, impaired bladder emptying, or the need for surgery. In current clinical practice, most patients are initially treated with medical therapy, usually with alpha-blockers. A minimally invasive treatment alternative is the use of urethral stents to preserve flow of urine from the bladder. Such stents are also associated with several problems such as encrustation, stone formation, pain, infection, migration and others. Another alternative is the gold standard treatment for managing benign prostatic hyperplasia; the trans urethral resection of prostate (TURP) surgery. Complications associate with TURP procedure include retrograde ejaculation, urinary incontinence, erectile dysfunction, urethral stricture, and others. The Butterfly Medical Prostatic Retraction Device is a definitive device intended for transurethral insertion into the male prostatic urethra diagnosed with Bladder Outlet Obstruction (BOO), caused by an enlarged prostate gland. It is a single use device intended to remain permanently in the prostate urethra, to open the occluded urethral passage. The Butterfly device has a specific shape adjusted to fit the prostatic urethral lumen, and is designed to reside only in the prostate urethra without migration to the urinary bladder or the bulbar urethra. Unlike other forms of treatment, the Butterfly device does not inflict any damage to the bladder neck, preventing irritation or retrograde ejaculation.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
92
The Butterfly device will be positioned and deployed with cystoscopy guidance
Shamir Medical Center
Be’er Ya‘aqov, Israel
Bnei Zion
Haifa, Israel
Rabin Medical Center
Petah Tikva, Israel
Ziv Medical Center
Safed, Israel
Reported device related adverse events
Assess the rate, nature and severity of device-related adverse events reported
Time frame: 12 months post procedure
Cystoscopic assessment - inflammation
Cystoscopic assessment to evaluate lack of local inflammation
Time frame: 12 months post procedure
Cystoscopic assessment - incrustations
Cystoscopic assessment to evaluate no incrustations
Time frame: 12 months post procedure
Cystoscopic assessment - implant coverage
Cystoscopic assessment to evaluate coverage by mucosa
Time frame: 12 months post procedure
Device migration
Rate of migration of the Butterfly device
Time frame: 12 months post procedure
Symptoms reduction - IPSS
Improvement in IPSS at 12 months compared to baseline
Time frame: Baseline to 12 months post procedure
Symptoms reduction - Qmax
Improvement in Qmax (by uroflowmetry) at 12 months compared to baseline
Time frame: Baseline to 12 months post procedure
Sexual quality of life evaluation - erectile dysfunction
Rate of de-novo sustained erectile dysfunction
Time frame: 12 month post procedure
Sexual quality of life evaluation - retrograde ejaculation
Rate of de-novo sustained retrograde ejaculation
Time frame: 12 month post procedure
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