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Retrospective, Non-significant Risk, Deep Brain Stimulation (DBS) Care Management Software Feasibility Study

NCT01750242 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 20

Last updated 2024-06-03

Study results available
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Summary

To evaluate DBS device settings and match with the features of the DBS care management software.

Conditions

Interventions

DEVICE

Medtronic DBS system

Advanced Parkinson's disease patients implanted with the Medtronic Deep Brain Stimulation (DBS) system.

Sponsors & Collaborators

  • MedtronicNeuro

    lead INDUSTRY

Principal Investigators

  • Rajesh Pahwa, MD · Parkinson's Disease and Movement Disorder Center, University of Kansas Medical Center

  • Melissa Houser, MD · Scripps Clinic Division of Neurology

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-11-30
Primary Completion
2013-05-31
Completion
2013-08-31

Countries

  • United States

Study Locations

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Entities

Diseases

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 NCT01750242 on ClinicalTrials.gov