Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT01643213 · ClinicalTrials.gov registry record · NA

Randomized Study of Failed SCS Trials Comparing Outcomes Using the Observational Mechanical Gateway (OMG) Connector

A NA study, sponsored by Boston Scientific Corporation.

Completed
Registry status
NA
Development phase
27
Enrollment target

NCT01643213: Completed NA study, sponsored by Boston Scientific Corporation.

NCT01643213 is a NA study that has completed, run by Boston Scientific Corporation. The registered enrollment target is 27 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT01643213, a NA study, has completed, sponsored by Boston Scientific Corporation.

COMPLETED
Registry status
NA
Development phase
27 participants
Enrollment target

Study Summary

The purpose of this study is to evaluate patient preference of the Boston Scientific Corporation (BSC) commercially approved spinal cord stimulation (SCS) systems with the Observational Mechanical Gateway (OMG) in patients who failed non-BSC SCS trial therapy.

Primary Outcome

Subject were asked if he/she prefers their current period SCS therapy over the SCS therapy he/she received during the SCS trial period prior to Baseline

Interventions

  • DEVICE Non Boston Scientific SCS Trial Therapy
  • DEVICE BSC approved SCS Trial Therapy w/ OMG

Trial Details

FieldValue
Enrollment Target 27 participants
Start Date 2012-07
Est. Completion 2015-02
Phase NA
Boston Scientific Corporation

280 total trials

What the finished NCT01643213 record still lists

NCT01643213 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 27 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower).

The record links to 0 conditions, and to 2 interventions - of which Non Boston Scientific SCS Trial Therapy is the first listed.

NCT01643213 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01643213 about?

NCT01643213 is a clinical study titled "Randomized Study of Failed SCS Trials Comparing Outcomes Using the Observational Mechanical Gateway (OMG) Connector". The purpose of this study is to evaluate patient preference of the Boston Scientific Corporation (BSC) commercially approved spinal cord stimulation (SCS) systems with the Observational Mechanical Gateway (OMG) in patients who failed non-BSC SCS trial therapy.

What is the current status of trial NCT01643213?

This trial is currently completed. It is a NA study. The enrollment target is 27 participants. The study started on 2012-07. Estimated completion is 2015-02.

What interventions are being tested in trial NCT01643213?

The interventions under investigation include: Non Boston Scientific SCS Trial Therapy (DEVICE), BSC approved SCS Trial Therapy w/ OMG (DEVICE).

Who is sponsoring clinical trial NCT01643213?

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 NCT01643213's enrollment target sits among peer trials

27 1708th of 2000 higher than 291 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

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT00912041 · 27 participants · NA

    BrainGate2: Feasibility Study of an Intracortical Neural Interface System for Persons With Tetraplegia

  • NCT02847559 · 27 participants · Phase 2

    Optune Delivered Electric Field Therapy and Bevacizumab in Treating Patients With Recurrent or Progressive Grade 2 or 3 Meningioma

  • NCT03380195 · 27 participants · NA

    Effects of Watermelon Juice on Heart Rate Recovery and Post-exercise Muscle Soreness

  • NCT03384238 · 27 participants · Phase 1

    Panitumumab-IRDye800 in Patients With Pancreatic Cancer Undergoing Surgery

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT01643213, the US trial registry maintained by the National Library of Medicine. NCT01643213 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.