Secondary Procedures for the Treatment of Stress Urinary Incontinence


About this study


  1. To construct a cohort of women who underwent a stress urinary incontinence surgery from January 1, 2002 through February 28, 2012.

  2. To report on the treatment outcome after surgical intervention and compare outcomes between different types of surgeries.

  3. To report on the outcomes for surgical treatment of recurrent stress urinary incontinence after failed 1st surgical attempt and to compare different types of surgical interventions for the 2nd surgery.


Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Please contact the study team to discuss whether or not you are eligible to participate in a study.

Inclusion Criteria:       

Participants:  all patients who have undergone 2 or more surgeries for the treatment of SUI before February 28, 2012. Patients must have at least one surgery done at Mayo Clinic Rochester MN.


Exclusion Criteria:      

Patients with ≤1 surgery for SUI.

Patients < 21 years of old.

Patients with neurologic disease/injuries that affect their urinary continence

Patients with a urethral diverticulum

Patients who declined research authorization

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location Status Contact

Rochester, Minn.

Mayo Clinic principal investigator

Emanuel Trabuco, M.D.

Closed for enrollment

Contact information:

Emanuel Trabuco M.D.

(507) 538-8400

More information


Publications are currently not available

Study Results Summary

Not yet available

Supplemental Study Information

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