InterStim® Amplitude Study
NCT03335761 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 97
Last updated 2021-01-08
Summary
This feasibility study will explore the effects of three different InterStim amplitude settings on overactive bladder symptoms (OAB).
Conditions
- Urinary Urge Incontinence
Interventions
- DEVICE
-
InterStim Therapy
Device Programming
Sponsors & Collaborators
-
MedtronicNeuro
lead INDUSTRY
Study Design
- Allocation
- RANDOMIZED
- Purpose
- BASIC_SCIENCE
- Masking
- SINGLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Sex
- FEMALE
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2018-02-27
- Primary Completion
- 2019-11-06
- Completion
- 2019-11-06
- FDA Device
- Yes
Countries
- United States
- Belgium
- Canada
- France
- Italy
- Netherlands
- United Kingdom
Study Locations
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