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Previously Implanted Pudendal Nerve Stimulation

NCT04473469 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 5

Last updated 2024-06-03

Study results available
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Summary

This study seeks to examine the response of the bladder to different pudendal nerve stimulation frequencies, by studying patients who have been previously-implanted with pudendal nerve neurostimulators.

Conditions

  • Urinary Retention
  • Underactive Bladder

Interventions

DEVICE

Medtronic Interstim II Model 3058 Neurostimulator

Patients will undergo stimulation of the pudendal nerve. All stimulation parameters used will be within the normal hard-coded limits of the implantable pulse generator (IPG).

Sponsors & Collaborators

Principal Investigators

  • Tim Bruns, Ph.D. · University of Michigan

  • Priyanka Gupta, M.D. · University of Michigan

Study Design

Allocation
NA
Purpose
BASIC_SCIENCE
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-01-19
Primary Completion
2023-05-02
Completion
2023-05-02
FDA Device
Yes

Countries

  • United States

Study Locations

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Entities

Companies

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 NCT04473469 on ClinicalTrials.gov