Memokath® 044TW Stent for Treatment of Urethral Stricture

Patients with bulbar urethral stricture are 2:1 randomised for either urethral dilation or internal urethrotomy with (treatment group) or without (control group) subsequent stenting. All patients are followed for up to one year at 4-6 weeks, 3, 6, 9 and 12 months with visual assessment (urethroscopy) of urethral patency at the treated segment of the urethra. The stent is removed at one year. In case of premature stent removal the patient is also followed for up to one year unless further intervention is decided.

Control patients are offered the stent treatment option if the stricture recurs within the observation period but this group is separately analysed.

Inclusion criteria

• Males > 21 years of age
• Recurrent stricture of the bulbar urethra:

• < 50 mm in length on urethrography; and which
• has a segment unable to accommodate a 16Fr flexible cystoscope
• Healthy tissue on both sides of stent
• Urinary flow in the abnormal range of the Siroky nomogram.
• Written informed consent obtained prior to participation in the study
• Patients must be available for all follow-up visits.

Exclusion criteria

• Strictures:

• outside the bulbous urethra
• associated with, or suspected to be, urethral carcinoma
• secondary to pelvic distraction injuries
• Inability to enlarge the bulbar urethral stricture to > 26 Fr.
• Presence of any other urologic implant
• Presence of urethral diverticuli
• History of hypospadias repair
• Presence or prior history of balanitis xerotica obliterans.
• Uncontrolled bleeding disorder
• Active urinary tract infection
• Any urological condition that would be likely to require additional urethral instrumentation during the period of the investigation, including, but not limited to, benign prostatic hypertrophy requiring treatment; use of alpha blockers; active prostate cancer; an unevaluated elevated prostate-specific antigen (PSA); bladder malignancy; or any recurrent urinary stone formation.
• Serum creatinine > 2.0 mg/dl or evidence of progressive renal disease
• Concurrent participation in another clinical investigation
• Current illness that might confound the results of this investigation
• Inability to participate in all of the necessary study activities
• Inability or unwillingness to return for all required follow-up visits
• Inability or unwillingness to sign the patient informed consent document