NL-OMON46734
Completed
Phase 4
Evaluation of the patients* satisfaction and safety of a non-degradable urethral bulking agent for female stress urinary incontinence - Euro study
Overview
- Phase
- Phase 4
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Academisch Medisch Centrum
- Enrollment
- 75
- Status
- Completed
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •\- \> 18 years
- •\- who underwent treatment with bulkinjection therapy Urolastic for stress urinary incontinence
Exclusion Criteria
- •Incapable of giving informed consent
Outcomes
Primary Outcomes
Not specified
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