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NCT01990287 · ClinicalTrials.gov registry record · NA
SENSE (Subcutaneous and Epidural Neuromodulation System Evaluation) Study
A NA study, sponsored by Abbott Medical Devices.
- Terminated
- Registry status
- NA
- Development phase
- 38
- Enrollment target
NCT01990287 is a NA study that was terminated before completion, run by Abbott Medical Devices. The registered enrollment target is 38 participants.
The verdict
NCT01990287, a NA study, was terminated before completion, sponsored by Abbott Medical Devices.
- TERMINATED
- Registry status
- NA
- Development phase
- 38 participants
- Enrollment target
Study Summary
The purpose of the study is to demonstrate safety and efficacy of spinal cord stimulation with peripheral nerve field stimulation for the treatment of chronic low back and leg pain.
Interventions
- DEVICE SCS and PNfS
- DEVICE SCS Alone
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 38 participants |
| Start Date | 2013-11 |
| Est. Completion | 2016-02 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01990287
The ClinicalTrials.gov registry entry for NCT01990287 describes a study currently listed as terminated, categorized as NA. The registered enrollment target is 38 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Abbott Medical Devices, which has 261 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which SCS and PNfS is the first listed.
NCT01990287 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT01990287 about?
NCT01990287 is a clinical study titled "SENSE (Subcutaneous and Epidural Neuromodulation System Evaluation) Study". The purpose of the study is to demonstrate safety and efficacy of spinal cord stimulation with peripheral nerve field stimulation for the treatment of chronic low back and leg pain.
What is the current status of trial NCT01990287?
This trial is currently terminated. It is a NA study. The enrollment target is 38 participants. The study started on 2013-11. Estimated completion is 2016-02.
What interventions are being tested in trial NCT01990287?
The interventions under investigation include: SCS and PNfS (DEVICE), SCS Alone (DEVICE).
Who is sponsoring clinical trial NCT01990287?
This trial is sponsored by Abbott Medical Devices, which has 261 total clinical trials registered on ClinicalTrials.gov.
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