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NCT01213251 · ClinicalTrials.gov registry record · Phase 2
Post-Myocardial Infarction Remodeling Prevention Therapy
A Phase 2 study, sponsored by Medtronic Cardiac Rhythm and Heart Failure.
- Completed
- Registry status
- Phase 2
- Development phase
- 129
- Enrollment target
NCT01213251: Completed Phase 2 study, sponsored by Medtronic Cardiac Rhythm and Heart Failure.
NCT01213251 is a Phase 2 study that has completed, run by Medtronic Cardiac Rhythm and Heart Failure. The registered enrollment target is 129 participants, roughly in line with the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01213251, a Phase 2 study, has completed, sponsored by Medtronic Cardiac Rhythm and Heart Failure.
- COMPLETED
- Registry status
- Phase 2
- Development phase
- 129 participants
- Enrollment target
Study Summary
The purpose of this study is to demonstrate the feasibility of pacing as a therapy to prevent adverse remodeling of the myocardium following an acute myocardial infarction (MI) in patients at highest risk for adverse myocardial remodeling.
Primary Outcome
Left ventricular end diastolic volume (LVEDV) was measured by echocardiogram. Change was measured as Month 18 LVEDV minus baseline LVEDV. Per protocol, change in LVEDV is compared between Pooled Pacing (Single site + Dual Site) and Control.
Interventions
- DEVICE Single Site Pacing
- DEVICE Dual Site Pacing
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 129 participants |
| Start Date | 2010-12 |
| Est. Completion | 2016-04 |
| Phase | Phase 2 |
What the finished NCT01213251 record still lists
NCT01213251 is an interventional study that assigns participants to a tested intervention. The registered 129 participants enrollment target is mid-sized for trials with a published cap, roughly in line with the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target.
The record links to 0 conditions, and to 2 interventions - of which Single Site Pacing is the first listed.
NCT01213251 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01213251 about?
NCT01213251 is a clinical study titled "Post-Myocardial Infarction Remodeling Prevention Therapy". The purpose of this study is to demonstrate the feasibility of pacing as a therapy to prevent adverse remodeling of the myocardium following an acute myocardial infarction (MI) in patients at highest risk for adverse myocardial remodeling.
What is the current status of trial NCT01213251?
This trial is currently completed. It is a Phase 2 study. The enrollment target is 129 participants. The study started on 2010-12. Estimated completion is 2016-04.
What interventions are being tested in trial NCT01213251?
The interventions under investigation include: Single Site Pacing (DEVICE), Dual Site Pacing (DEVICE).
Who is sponsoring clinical trial NCT01213251?
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 NCT01213251's enrollment target sits among peer trials
129 553rd of 2000 higher than 1,448 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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