MedTrace Logo

Patient Registry to Study the Tined Lead Used With the InterStim System For Urinary Control

NCT00225966 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 153

Last updated 2013-11-15

No results posted yet for this study

Summary

The purpose of this study is assess the long-term safety and effectiveness of the InterStim tined lead using a minimally invasive approach.

Conditions

  • Urge Incontinence
  • Urinary Retention

Interventions

DEVICE

Device Medtronic InterStim Tined Leads Models 3889 and 3093

Sponsors & Collaborators

  • MedtronicNeuro

    lead INDUSTRY

Principal Investigators

  • Medtronic Investigator · Medtronic

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
16 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2004-08-31
Completion
2007-10-31

Countries

  • United States

Study Locations

More Related Trials

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 NCT00225966 on ClinicalTrials.gov