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AdVance® vs ARGUS® Sling Procedure in Male With Post Prostatectomy Stress Urinary Incontinence

NCT01866085 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 128

Last updated 2013-05-31

No results posted yet for this study

Summary

The study is designed to assess efficacy and subject satisfaction of two sling devices: Advance and Argus, in male patients with stress urinary incontinence after prostatectomy.

Conditions

  • Stress Urinary Incontinence

Interventions

PROCEDURE

AdVance® sling procedure

PROCEDURE

ARGUS Sling procedure

Sponsors & Collaborators

  • Center Hospitalier de Fleurimont,Sherbrooke University

    collaborator UNKNOWN

  • Sunnybrook Health Sciences Centre

    collaborator OTHER

  • Jewish General Hospital

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
MALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-06-30
Primary Completion
2014-06-30
Completion
2015-06-30

Countries

  • Canada

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01866085 on ClinicalTrials.gov