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Clinical trial intelligence report
Evaluating the Change of Overactive Bladder Symptoms in Women Post Pubovaginal Sling Procedure for Stress Incontinence
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jun 24, 2026
Report code
NCT01194999-Jun 24, 2026
NCT ID
NCT01194999
Status
COMPLETED
Phase
Phase 4
Sponsor
Barrie Urology Associates
Executive brief
Investment-Ready Snapshot
The study conducted by Barrie Urology Associates evaluates the impact of the Pubovaginal Sling (PVS) procedure on Overactive Bladder (OAB) symptoms in women post-surgery. Given the prevalence of stress urinary incontinence and the potential for PVS to alleviate OAB symptoms, this research could position Barrie Urology Associates as a leader in surgical interventions for female urinary incontinence. The findings may influence market dynamics by validating PVS as a dual-purpose treatment, potentially increasing its adoption and driving competition against other OAB management therapies, including pharmacological options. Diligence should focus on the clinical outcomes and patient satisfaction metrics to assess market entry strategies and partnerships, particularly with industry collaborators like Astellas Pharma Canada, Inc.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT01194999
Indication
Urinary Bladder, Overactive
Modality
medical device
Target
Overactive Bladder Symptoms Management
Intervention
Pubovaginal sling procedure
Source record
Protocol Description
Detailed source ingestion pending.
Source record
Outcome Measures
Detailed source ingestion pending.
Source record
Eligibility
Detailed source ingestion pending.
AI analysis
Known Results And Readout Context
Detailed source ingestion pending.
IP intelligence
Patent And IP Landscape
Detailed source ingestion pending.
Source record
Contacts
Detailed source ingestion pending.