Clinical Research Directory

Inclusion Criteria: 1. The subject has agreed to be treated with the male Incontinence surgery devices 2. The subject is willing and able to give valid informed consent. 3. The subject is \> 18 years of age. 4. The subject has confirmed stress urinary incontinence for at least 12 months after prostatectomy or radiotherapy. 5. It has been confirmed the stress urinary incontinence with 24-Hour Pad Weight test 6. Pre-operative urodynamic assessment and flexible cystoscopy were performed in all cases 7. The subject is willing and able to return for follow-up evaluations and questionnaire completion according to the study protocol. 8. There are no surgical contraindications. Exclusion Criteria: 1. The subject has an active urinary tract infection or active skin infection in region of surgery 2. The subject has serious bleeding disorders 3. The subject has unstable bladder neck stricture disease 4. The subject has Neurogenic bladder condition that is not treatable or controllable by pharmacological or alternative methods. 5. The subject has Detrusor-external sphincter dyssynergia. 6. The subject is unable or unwilling to sign the informed consent form (ICF)and/or comply with all follow-up requirements according to the study protocol 7. The subject is likely to undergo radiation therapy within the next 6 months 8. The subject has a history of connective tissue or autoimmune conditions. 9. The subject has a compromised immune system. 10. The subject has renal insufficiency, and upper and/or lower urinary tract relative obstruction. 11. The subject's reading level is judged inadequate for reading and understanding the quality of life questionnaires and other study materials