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NCT01625104 · ClinicalTrials.gov registry record · NA
Randomized Trial of a Quality Improvement Intervention to Decrease D2B Time in Primary PCI for AMI
A NA study, sponsored by University of Michigan.
- Completed
- Registry status
- NA
- Development phase
- 882
- Enrollment target
NCT01625104: Completed NA study, sponsored by University of Michigan.
NCT01625104 is a NA study that has completed, run by University of Michigan. The registered enrollment target is 882 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (37% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01625104, a NA study, has completed, sponsored by University of Michigan.
- COMPLETED
- Registry status
- NA
- Development phase
- 882 participants
- Enrollment target
Study Summary
The primary objective of this study is to assess whether an aggressive quality improvement intervention strategy will decrease time from hospital presentation to first balloon inflation in non-transfer patients with acute ST segment elevation MI (STEMI) treated with primary percutaneous coronary intervention (PCI). Twelve hospitals in Michigan were randomized to either aggressive intervention or control. The intervention consisted of Grand Rounds at each hospital, sharing of best practices, and coordinating center staff working closely with staff at each intervention hospital to discuss solutions to barriers to rapid treatment for STEMI patients.
Primary Outcome
Arrival time in Emergency Department to first balloon inflation in the coronary artery. Any reduction in median Door to Balloon Time from baseline to follow-up was counted as reduction in time
Interventions
- OTHER Non Intervention
- OTHER Agressive Intervention Process Improvement Strategies
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 882 participants |
| Start Date | 2003-09 |
| Est. Completion | 2006-12 |
| Phase | NA |
What the finished NCT01625104 record still lists
NCT01625104 is an interventional study that assigns participants to a tested intervention. The registered 882 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (37% lower).
The record links to 0 conditions, and to 2 interventions - of which Non Intervention is the first listed.
NCT01625104 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01625104 about?
NCT01625104 is a clinical study titled "Randomized Trial of a Quality Improvement Intervention to Decrease D2B Time in Primary PCI for AMI". The primary objective of this study is to assess whether an aggressive quality improvement intervention strategy will decrease time from hospital presentation to first balloon inflation in non-transfer patients with acute ST segment elevation MI (STEMI) treated with primary percutaneous coronary int...
What is the current status of trial NCT01625104?
This trial is currently completed. It is a NA study. The enrollment target is 882 participants. The study started on 2003-09. Estimated completion is 2006-12.
What interventions are being tested in trial NCT01625104?
The interventions under investigation include: Non Intervention (OTHER), Agressive Intervention Process Improvement Strategies (OTHER).
Who is sponsoring clinical trial NCT01625104?
This trial is sponsored by University of Michigan, which has 1,327 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT01625104's enrollment target sits among peer trials
882 130th of 2000 higher than 1,871 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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