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Completed Not applicable Interventional Results available

InterStim® Amplitude Study

ClinicalTrials.gov ID: NCT03335761

Public ClinicalTrials.gov record NCT03335761. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 24, 2026, 4:53 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This feasibility study will explore the effects of three different InterStim amplitude settings on overactive bladder symptoms (OAB).

Study identification

NCT ID
NCT03335761
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
MedtronicNeuro
Industry
Enrollment
97 participants

Conditions and interventions

Interventions

Device

Eligibility (public fields only)

Age range
18 Years and older
Sex
Female
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Feb 27, 2018 (Actual)
Primary completion
Nov 6, 2019 (Actual)
Completion
Nov 6, 2019 (Actual)
Last update posted
Jan 8, 2021

2018 – 2019

United States locations

U.S. sites
12
U.S. states
8
U.S. cities
12
Facility City State ZIP Site status
Academic Urology & Urogynecology of Arizona Phoenix Arizona 85027 —
East Coast Institute for Research Jacksonville Florida 32216 —
Pinellas Urology St. Petersburg Florida 33710 —
Florida Urology Partners Tampa Florida 33606 —
Minnesota Urology Fridley Fridley Minnesota 55432 —
Minnesota Urology Woodbury Woodbury Minnesota 55125 —
Adult Pediatric Urology and Urogynecology Omaha Nebraska 68114 —
Urologic Research & Consulting Englewood New Jersey 07631 —
Carolina Urology Partners Concord North Carolina 28025 —
Chattanooga Hamilton County Hospital Authority d/b/a Erlanger Health System Chattanooga Tennessee 37421 —
Vanderbilt University Medical Center Nashville Tennessee 37232-2765 —
Aurora Research Institute - Aurora West Allis Women's Pavilion West Allis Wisconsin 53227 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 6 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03335761, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jan 8, 2021 · Synced Oct 24, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03335761 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →