Secondary Procedures for the Treatment of Stress Urinary Incontinence

Overview

About this study

Aims:

To construct a cohort of women who underwent a stress urinary incontinence surgery from January 1, 2002 through February 28, 2012.
To report on the treatment outcome after surgical intervention and compare outcomes between different types of surgeries.
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. Contact the study team to discuss study eligibility and potential participation.

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
Rochester, Minn. Mayo Clinic principal investigator Emanuel Trabuco, M.D.	Closed for enrollment

Mayo Clinic Location

Status

Rochester, Minn.

Mayo Clinic principal investigator

Emanuel Trabuco, M.D.

Closed for enrollment

More information

Publications

Publications are currently not available

Clinical Trials