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InterStim® Sacral Nerve Modulation Cycling Study

NCT01957137 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 30

Last updated 2017-12-12

Study results available
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Summary

The study will assess the effects of different InterStim cycling settings on urinary urge incontinence.

Conditions

  • Urinary Urge Incontinence

Interventions

DEVICE

InterStim® (Device Programming)

Sponsors & Collaborators

  • MedtronicNeuro

    lead INDUSTRY

Principal Investigators

  • Steven W Siegel, MD · Metro Urology

  • Shaw Zhou, MD · Pinellas Urology, Inc.

  • Karl Kreder, Jr., MD, MBA · University of Iowa Healthcare

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-09-30
Primary Completion
2015-11-30
Completion
2015-11-30

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01957137 on ClinicalTrials.gov