Informations générales (source: ClinicalTrials.gov)
Prospective Interventional Safety and Efficacy Study of USTRAP™ in Male Urinary Incontinence. an Open, Randomised, Multicentre Study Versus Artificial Sphincter. (PROSPECT)
Interventional
N/A
Quanta Medical (Voir sur ClinicalTrials)
juin 2018
décembre 2026
26 avril 2025
Few surgical methods to treat male stress urinary incontinence have been assessed in
comparative, randomised interventional studies.
Ustrap is a new adjustable-pressure 4-arm device. The artificial sphincter is currently
considered the gold standard device in this field.
The aim of this randomised prospective international study is to assess the efficacy and
safety of the Ustrap® device comparatively with an artificial sphincter (AMS800) in the
treatment of stress urinary incontinence following prostate removal in cancer patients.
Etablissements
| Les établissements d'Île-de-France ayant mis à jour leurs données Origine et niveau de fiabilité des données | |||||
|---|---|---|---|---|---|
| HOPITAL FOCH | FLORENCE COUR | 05/05/2025 07:11:58 | Contacter | ||
| Les établissements sans correspondance certaine dans le répertoire FINESS dont les données sont issues de ClinicalTrials.gov Origine et niveau de fiabilité des données | |||||
| CHU Charles Nicolle - 76031 - Rouen - France | Contact (sur clinicalTrials) | ||||
Critères
Homme
Inclusion Criteria:
Disease-related criteria:
- persistent urinary incontinence >= 12 months following radical prostatectomy for
prostate adenocarcinoma
- presenting an indication for surgical insertion of a medical device
- 24h PAD test > 100 g per day
- controlled prostate adenocarcinoma, with PSA ≤ 1 ng/ml
Population-related criteria:
- male subjects aged 18 years and over
- having provided free, informed written consent to take part in the study
- patients independent and able to use the collar without difficulty and able to
manage an artificial sphincter
- Patient able to understand and sign the consent form and to complete questionnaires
- Patient without mental impairment
- Patients belonging to or covered by Social Security.
Disease-related criteria:
- persistent urinary incontinence >= 12 months following radical prostatectomy for
prostate adenocarcinoma
- presenting an indication for surgical insertion of a medical device
- 24h PAD test > 100 g per day
- controlled prostate adenocarcinoma, with PSA ≤ 1 ng/ml
Population-related criteria:
- male subjects aged 18 years and over
- having provided free, informed written consent to take part in the study
- patients independent and able to use the collar without difficulty and able to
manage an artificial sphincter
- Patient able to understand and sign the consent form and to complete questionnaires
- Patient without mental impairment
- Patients belonging to or covered by Social Security.
Disease-related criteria:
- Documented neurological bladder or history of neurological disease liable to
interfere with urinary symptoms.
- Presence of urethral anastomotic stenosis preventing passage of the fiberscope at
the initial endoscopy
- Severe symptomatic hyperactive or hypoactive bladder not controlled by drug therapy
- Severe constitutional haemorrhagic disease or haemophilia
- Patients presenting urinary infection not controlled
- Patients presenting severe renal failure and obstructive pathologies of the upper
urinary tract with severe renal failure.
- Patients presenting deep immune deficiency
- Patient presenting recto-urethral fistula
- Patient with tumor of bladder
- Patient having bladder stones with failure of bladder stone treatment
Criteria related to incontinence treatment:
- Allergy to any of the components of the medical devices
- History of surgery to insert a medical device for treatment of incontinence (e.g.
artificial sphincter, suburethral strap, continence balloons, etc.)
- History of periurethral injection of filling agents
- Inability to use either of the study devices
- Drug treatment: duloxetine or any treatment likely to modify continence results
- Not receiving and not likely to receive radiotherapy at any time throughout the
12-month follow-up period Population-related criteria
- Foreseeable unavailability during the study . Patient deprived of liberty by
administrative or judicial decision or under legal guardianship
- Participation in another clinical trial in the 3 months preceding the initial visit