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INJECTABLE BULKING AGENT FOR MALE URINARY INCONTINENCE TREATMENT: A MULTI-CENTRE EFFECTIVENESS AND SAFETY PILOT STUDY

Hypothesis: Opsys will improve mild incontinence based on urine loss per 24 h measured by 24 h pad test.The main objective of this study is to test the effectiveness of Opsys in a group of selected subjects with minimal to mild (less than 30 g per…

The European Study of Altis® Single Incision Sling System for Female Stress Urinary Incontinence;A prospective, post-market, single arm, multicenter comparing baseline data to the 12 and 36 month data in 136 patients with stress urinary incontinence

Primary goal:The cure at 12 monthsSecondary goals:1. Cough Stress Test (HST): objective endpoint2. Question 3 of the UDI-6 questionnaire: subjective endpoint3. Primary endpoint at 6 weeks, 6 months, and 36 months 24maanden4. Reduction of urine loss…

Levobupivacaine for pediatric caudal block. Comparison of three different dose in children undergoing hypospadia repair: a double-blinded randomised study

To determine the best doses-respons of levobupivacaine for postoperatief analgesia after caudal anesthesia for hypospadia repair.