Fundación IVO Registry for Patients Undergoing Sling or Artificial Urinary Sphincter After Prostate Cancer Treatment

Inclusion criteria

• The subject has agreed to be treated with the male Incontinence surgery devices
• The subject is willing and able to give valid informed consent.
• The subject is \> 18 years of age.
• The subject has confirmed stress urinary incontinence for at least 12 months after prostatectomy or radiotherapy.
• It has been confirmed the stress urinary incontinence with 24-Hour Pad Weight test
• Pre-operative urodynamic assessment and flexible cystoscopy were performed in all cases
• The subject is willing and able to return for follow-up evaluations and questionnaire completion according to the study protocol.
• There are no surgical contraindications.

Exclusion criteria

• The subject has an active urinary tract infection or active skin infection in region of surgery
• The subject has serious bleeding disorders
• The subject has unstable bladder neck stricture disease
• The subject has Neurogenic bladder condition that is not treatable or controllable by pharmacological or alternative methods.
• The subject has Detrusor-external sphincter dyssynergia.
• 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
• The subject is likely to undergo radiation therapy within the next 6 months
• The subject has a history of connective tissue or autoimmune conditions.
• The subject has a compromised immune system.
• The subject has renal insufficiency, and upper and/or lower urinary tract relative obstruction.
• The subject's reading level is judged inadequate for reading and understanding the quality of life questionnaires and other study materials