Long-term Evaluation of the I-STOP Sling in Stress Urinary Incontinence Treatment
ConditionStress Urinary Incontinence (SUI)
Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age18+
SponsorDILO Medical
About this trial
Evaluate quality of life and rate of reoperation after implantation of the I-STOP sling for stress urinary incontinence
Eligibility criteria
Qualifiers
Adult woman aged over 18 ;
Patient with SUI, having escaped "conservative" medical treatment, with indication for surgical treatment with implantation of an I-STOP® strip via trans-obturator or retropubic route as indicated in the instructions for use of the SUI implant ;
Patient affiliated to a social security scheme;
Patient capable of completing a self-questionnaire;
Disqualifiers
Minor patient, pregnant or breastfeeding ;
Adult patient subject to a measure of legal protection, guardianship, curatorship or deprived of liberty by judicial or administrative decision ;
Patient presenting a contraindication to the use of the implant indicated in the instructions for use of the implant ;
Patient with a medical contraindication to surgery and/or anaesthesia.
Trial design
Treatments tested in this trial
- Not listed
Trial groups
No trial groups listed
Locations
Sponsors and collaborators
Source ClinicalTrials.gov