NCT01799122.

Study name	Randomized clinical trial comparing Mini‐Arc Precise Pro and the trans vaginal obturator tape for surgical management of stress urinary incontinence
Methods	Design: RCT
Participants	Enrolment: NR Country: Canada Setting: unclear (Manitoba; no further details) Inclusion criteria: 25 years or older; women with SUI with a positive cough test result; patient requesting treatment with surgery Exclusion criteria: predominantly OAB; previous failed procedure; MUCP < 20 cm H2O; presence of vaginal prolapse stage > 1; voiding dysfunction (PVR > 100 mL)
Interventions	Group I: MiniArc Precise Pro Group II: TVT‐O
Outcomes	Primary outcome Cough test: assessed 1 year from surgery Secondary outcomes Subjective symptoms: assessed 1 year and 2 years postoperatively Quality‐of‐life questionnaires: assessed 1 year and 2 years postoperatively
Starting date	NR (first posted 26 February 2013)
Contact information	Ken Maslow Tel: 204‐235‐3039 Email: maslow@sbgh.mb.ca
Notes	Follow‐up time: 1 year and 2 years Sponsors and collaborators: University of Manitoba