Using the Gynecare MoniTorr* device to measure urethral pressure before incontinence surgery

The measurement of urethral pressure with the MoniTORR* device to predict outcome after urinary incontinence surgery based on urodynamics studies at 6 months.

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

ANZCTR

Registry ID

ACTRN12605000182695

Enrollment

120

Registered

2005-08-19

Start date

2005-04-24

Completion date

Unknown

Last updated

2020-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Urethral retro-resistance pressure (URP)measurement.

Eligibility

Sex/Gender

All

Age

0 to No maximum

Healthy volunteers

Inclusion criteria

Women with urodynamics stress incontinence undergoing a TVT procedure at the two study centres. Concomitant prolapse surgery is not a contraindication. Willingness to participate.

Exclusion criteria

Medically unfit for surgery. Refusal to participate. Patients who are recommended surgery other than TVT (e.g. Colposuspension, Sling, Bulking agent, Transobturator procedure).

Outcome results