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NCT02087046 · ClinicalTrials.gov registry record · NA

Deep Brain Stimulation (DBS) for the Suppression of Tremor

A NA study, sponsored by Abbott Medical Devices.

Completed
Registry status
NA
Development phase
127
Enrollment target

NCT02087046: Completed NA study, sponsored by Abbott Medical Devices.

NCT02087046 is a NA study that has completed, run by Abbott Medical Devices. The registered enrollment target is 127 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (91% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02087046, a NA study, has completed, sponsored by Abbott Medical Devices.

COMPLETED
Registry status
NA
Development phase
127 participants
Enrollment target

Study Summary

The purpose of the proposed study is to demonstrate the safety and efficacy of the ANS Totally Implantable Deep Brain Stimulation System in the VIM nucleus of the thalamus implanted for the treatment of tremor due to essential tremor. This study will be included in the Pre-Market Approval Application to support the safety of this device in use.

Primary Outcome

The Fahn, Tolosa, Marin Tremor Rating Scale (referred to as the CRST), is a rating tool to assess the severity of postural, isometric, kinetic and task specific tremor in the dominant and non-dominant sides of the head, trunk and limbs of patients with ET. The CRST utilizes a 0 to 4 point scale where 0 indicates non-symptomatic (normal) and 4 indicates the most severe rating of the patient's tremor symptoms.

Interventions

  • DEVICE ANS Totally Implantable Deep Brain Stimulation System

Trial Details

FieldValue
Enrollment Target 127 participants
Start Date 2005-10
Est. Completion 2017-12
Phase NA
Abbott Medical Devices

261 total trials

What the finished NCT02087046 record still lists

NCT02087046 is an interventional study that assigns participants to a tested intervention. The registered 127 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (91% lower).

The record links to 0 conditions, and to 1 intervention - of which ANS Totally Implantable Deep Brain Stimulation System is the first listed.

NCT02087046 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02087046 about?

NCT02087046 is a clinical study titled "Deep Brain Stimulation (DBS) for the Suppression of Tremor". The purpose of the proposed study is to demonstrate the safety and efficacy of the ANS Totally Implantable Deep Brain Stimulation System in the VIM nucleus of the thalamus implanted for the treatment of tremor due to essential tremor. This study will be included in the Pre-Market Approval Applicati...

What is the current status of trial NCT02087046?

This trial is currently completed. It is a NA study. The enrollment target is 127 participants. The study started on 2005-10. Estimated completion is 2017-12.

What interventions are being tested in trial NCT02087046?

The interventions under investigation include: ANS Totally Implantable Deep Brain Stimulation System (DEVICE).

Who is sponsoring clinical trial NCT02087046?

This trial is sponsored by Abbott Medical Devices, which has 261 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02087046's enrollment target sits among peer trials

127 749th of 2000 higher than 1,252 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT02087046, the US trial registry maintained by the National Library of Medicine. NCT02087046 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.