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NCT00387244 · ClinicalTrials.gov registry record · NA

Efficacy of the Spinal Cord Stimulation System as Salvage Therapy

A NA study, sponsored by Boston Scientific Corporation.

Terminated
Registry status
NA
Development phase
7
Enrollment target

NCT00387244: Clinical Trial NA study, sponsored by Boston Scientific Corporation.

NCT00387244 is a NA study that was terminated before completion, run by Boston Scientific Corporation. The registered enrollment target is 7 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (100% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00387244, a NA study, was terminated before completion, sponsored by Boston Scientific Corporation.

TERMINATED
Registry status
NA
Development phase
7 participants
Enrollment target

Study Summary

The primary objective of this study is to evaluate the efficacy of spinal cord stimulation using the Precision implantable neurostimulation device for chronic and intractable pain of the trunk and or limbs in patients who have failed treatment with an intraspinal infusion pump or other SCS system.

Interventions

  • DEVICE Precision for Spinal Cord Stimulation

Trial Details

FieldValue
Enrollment Target 7 participants
Start Date 2006-08
Est. Completion 2008-04
Phase NA
Boston Scientific Corporation

280 total trials

Why NCT00387244 stopped before completion

NCT00387244 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 7 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (100% lower).

The record links to 0 conditions, and to 1 intervention - of which Precision for Spinal Cord Stimulation is the first listed.

NCT00387244 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00387244 about?

NCT00387244 is a clinical study titled "Efficacy of the Spinal Cord Stimulation System as Salvage Therapy". The primary objective of this study is to evaluate the efficacy of spinal cord stimulation using the Precision implantable neurostimulation device for chronic and intractable pain of the trunk and or limbs in patients who have failed treatment with an intraspinal infusion pump or other SCS system.

What is the current status of trial NCT00387244?

This trial is currently terminated. It is a NA study. The enrollment target is 7 participants. The study started on 2006-08. Estimated completion is 2008-04.

What interventions are being tested in trial NCT00387244?

The interventions under investigation include: Precision for Spinal Cord Stimulation (DEVICE).

Who is sponsoring clinical trial NCT00387244?

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 NCT00387244's enrollment target sits among peer trials

7 1982nd of 2000 higher than 18 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 NCT00387244, the US trial registry maintained by the National Library of Medicine. NCT00387244 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.