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COMPLETED

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

NCT01750242 · View on ClinicalTrials.gov ↗

Study Summary

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

Conditions Studied

Interventions

  • DEVICE Medtronic DBS system

Study Locations (2)

California

  • Scripps Clinic, Division of Neurology — La Jolla

Kansas

  • Parkinson's Disease and Movement Disorder Center, University of Kansas Medical Center — Kansas City

Trial Details

FieldValue
Enrollment Target 20 participants
Start Date 2012-11
Est. Completion 2013-08

Sponsor

MedtronicNeuro

14 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT01750242

The ClinicalTrials.gov registry entry for NCT01750242 describes a study currently listed as completed. It is categorized as an unspecified phase, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 20 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is MedtronicNeuro, which has 14 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Parkinson's Disease appearing as the primary indexed condition, and to 1 intervention — of which Medtronic DBS system is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT01750242 reports 2 study locations spanning 2 distinct geographic areas — top geographies include California, Kansas. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT01750242 about?

NCT01750242 is a clinical study titled "Retrospective, Non-significant Risk, Deep Brain Stimulation (DBS) Care Management Software Feasibility Study". To evaluate DBS device settings and match with the features of the DBS care management software.

What is the current status of trial NCT01750242?

This trial is currently completed. The enrollment target is 20 participants. The study started on 2012-11. Estimated completion is 2013-08.

What conditions does trial NCT01750242 study?

This clinical trial studies the following conditions: Parkinson's Disease. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT01750242?

The interventions under investigation include: Medtronic DBS system (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT01750242?

This trial is sponsored by MedtronicNeuro, which has 14 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT01750242 being conducted?

This trial has 2 study locations across California, Kansas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial