Urethral Length Measurement in Women Undergoing Suburethral Sling Operative Procedure

NCT01660438 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 188

Last updated 2016-05-20

No results posted yet for this study

Summary

This is a prospective, non-randomized, observational, multicenter study in which urethral length is measured in women with surgically-correctable stress urinary incontinence who undergo a suburethral sling operative procedure.

Conditions

  • Stress Urinary Incontinence

Sponsors & Collaborators

  • Cantonal Hospital, Frauenfeld

    lead OTHER

Principal Investigators

  • Volker Viereck, Prof. Dr. · Cantonal Hospital, Frauenfeld

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2010-08-31
Primary Completion
2013-02-28
Completion
2013-02-28

Countries

  • Germany
  • Poland
  • Switzerland

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 NCT01660438 on ClinicalTrials.gov