NCT01009333 - InterStim Therapy Programming Study | Biotech Hunter

Enrollment

Participants

Timeline

Start Date

November 30, 2009

Primary Completion Date

November 30, 2010

Study Completion Date

November 30, 2010

Conditions

Urgency FrequencyUrinary Urge Incontinence

Interventions

DEVICE

InterStim Therapy at rate 5.2 Hz

All subjects enrolled in this study were programmed to this rate setting for a 1-week period.

DEVICE

InterStim Therapy at rate 14 Hz

All subjects enrolled in this study were programmed to this rate setting for a 1-week period.

DEVICE

InterStim Therapy

All subjects enrolled in this study were programmed to each rate setting (low, medium, high) for a 1-week period.

Trial Locations (1)

Kenneth Peters, MD, Royal Oak