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NCT00386724 · ClinicalTrials.gov registry record · NA

Effectiveness of Precision Spinal Cord Stimulation With Artisan Paddle Electrode

A NA study, sponsored by Boston Scientific Corporation.

Terminated
Registry status
NA
Development phase
8
Enrollment target

NCT00386724: Clinical Trial NA study, sponsored by Boston Scientific Corporation.

NCT00386724 is a NA study that was terminated before completion, run by Boston Scientific Corporation. The registered enrollment target is 8 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00386724, a NA study, was terminated before completion, sponsored by Boston Scientific Corporation.

TERMINATED
Registry status
NA
Development phase
8 participants
Enrollment target

Study Summary

The primary objective of this study is to evaluate the acute and chronic efficacy of spinal cord stimulation using the Precision implantable neurostimulation device with the Artisan paddle electrode in patients with Failed Back Surgery Syndrome (FBSS) and associated primary or secondary back or lower extremity pain. There are significant numbers of patients with FBSS who have moderate to severe drug refractory pain. An optimal outcome will demonstrate that the Precision SCS device has significant effectiveness in reducing this pain resulting in improved quality of life and functional capacity.

Interventions

  • DEVICE Precision Spinal Cord Stimulation System
  • DEVICE Artisan Surgical Lead

Trial Details

FieldValue
Enrollment Target 8 participants
Start Date 2006-10
Est. Completion 2008-08
Phase NA
Boston Scientific Corporation

280 total trials

Why NCT00386724 stopped before completion

NCT00386724 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 8 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower).

The record links to 0 conditions, and to 2 interventions - of which Precision Spinal Cord Stimulation System is the first listed.

NCT00386724 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00386724 about?

NCT00386724 is a clinical study titled "Effectiveness of Precision Spinal Cord Stimulation With Artisan Paddle Electrode". The primary objective of this study is to evaluate the acute and chronic efficacy of spinal cord stimulation using the Precision implantable neurostimulation device with the Artisan paddle electrode in patients with Failed Back Surgery Syndrome (FBSS) and associated primary or secondary back or lowe...

What is the current status of trial NCT00386724?

This trial is currently terminated. It is a NA study. The enrollment target is 8 participants. The study started on 2006-10. Estimated completion is 2008-08.

What interventions are being tested in trial NCT00386724?

The interventions under investigation include: Precision Spinal Cord Stimulation System (DEVICE), Artisan Surgical Lead (DEVICE).

Who is sponsoring clinical trial NCT00386724?

This trial is sponsored by Boston Scientific Corporation, which has 280 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00386724's enrollment target sits among peer trials

8 1976th of 2000 higher than 19 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 NCT00386724, the US trial registry maintained by the National Library of Medicine. NCT00386724 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.