Clinical Trial

Optimization of Spontaneous Trial of Void in Women

Study Description

Optimization of Spontaneous Postoperative Trial of Void Among Women

Trial of void (TOV) is a diagnostic test performed on all women who undergo prolapse repair or incontinence surgery, due to the importance of diagnosing postoperative urinary retention (POUR). Incidence of POUR may be as high as 62% in some studies. Timely and accurate diagnosis is important to avoid complications such as urinary tract infection, bladder overdistension, and permanent bladder injury. Despite the frequent use of TOV, there is no gold standard for the test, and it likely has poor specificity, leading to discharge of more patients with catheter than required. This prospective cohort study will seek to establish evidence-based optimal parameters for spontaneous trial of void, a TOV modality that has merit for further evaluation given lower theoretical risk of urinary tract infection.

Location

Locations Selected Location

Methods

No pharmaceutical medication involved No pharmaceutical medication involved
Patients and healthy individuals accepted Patients and healthy individuals accepted

Procedure - PVR-based self-catheterization

Home self-catheterization based on standard of care

Additional Information

Official Study Title

Optimization of Spontaneous Trial of Void: a Prospective Cohort Study

Clinical Trial ID

NCT04010656

ParticipAid ID

e73x1e