InterStim Prospective Database

NCT00441935 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 736

Last updated 2017-12-26

No results posted yet for this study

Summary

The study is to collect information from patient charts and patient questionnaires to evaluate the effects of nerve stimulation therapy on urinary dysfunction.

Conditions

Interventions

DEVICE

Interstim Neuromodulation

Two stage procedure to implant an interstim device for neuromodulation.

Sponsors & Collaborators

  • William Beaumont Hospitals

    collaborator OTHER
  • Kenneth Peters, MD

    lead OTHER

Principal Investigators

  • Kenneth Peters, MD · William Beaumont Hospitals

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2004-04-30
Primary Completion
2016-12-16
Completion
2016-12-16

Countries

  • United States

Study Locations

More Related Trials

Entities

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 NCT00441935 on ClinicalTrials.gov