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NCT01112579 · ClinicalTrials.gov registry record · Phase 2
Determining the Feasibility of Spinal Cord Neuromodulation for the Treatment of Chronic Heart Failure
A Phase 2 study, sponsored by Medtronic Cardiac Rhythm and Heart Failure.
- Completed
- Registry status
- Phase 2
- Development phase
- 81
- Enrollment target
NCT01112579: Completed Phase 2 study, sponsored by Medtronic Cardiac Rhythm and Heart Failure.
NCT01112579 is a Phase 2 study that has completed, run by Medtronic Cardiac Rhythm and Heart Failure. The registered enrollment target is 81 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (39% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01112579, a Phase 2 study, has completed, sponsored by Medtronic Cardiac Rhythm and Heart Failure.
- COMPLETED
- Registry status
- Phase 2
- Development phase
- 81 participants
- Enrollment target
Study Summary
The purpose of this study is to determine the feasibility of spinal cord stimulation (SCS) as a chronic therapy for systolic heart failure.
Interventions
- DEVICE Medtronic PrimeADVANCED Neurostimulator
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 81 participants |
| Start Date | 2010-04 |
| Est. Completion | 2015-04 |
| Phase | Phase 2 |
What the finished NCT01112579 record still lists
NCT01112579 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 81 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (39% lower).
The record links to 0 conditions, and to 1 intervention - of which Medtronic PrimeADVANCED Neurostimulator is the first listed.
NCT01112579 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01112579 about?
NCT01112579 is a clinical study titled "Determining the Feasibility of Spinal Cord Neuromodulation for the Treatment of Chronic Heart Failure". The purpose of this study is to determine the feasibility of spinal cord stimulation (SCS) as a chronic therapy for systolic heart failure.
What is the current status of trial NCT01112579?
This trial is currently completed. It is a Phase 2 study. The enrollment target is 81 participants. The study started on 2010-04. Estimated completion is 2015-04.
What interventions are being tested in trial NCT01112579?
The interventions under investigation include: Medtronic PrimeADVANCED Neurostimulator (DEVICE).
Who is sponsoring clinical trial NCT01112579?
This trial is sponsored by Medtronic Cardiac Rhythm and Heart Failure, which has 115 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT01112579's enrollment target sits among peer trials
81 834th of 2000 higher than 1,159 of 2,000 other Phase 2 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 2 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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