N/A
N=882
Randomized Trial of a Quality Improvement Intervention to Decrease D2B Time in Primary PCI for AMI
STEMI
Bottom Line
View on ClinicalTrials.gov: NCT01625104 ↗Enrolled (actual)
882
Serious AEs
0.0%
Results posted
Dec 2017
Primary outcome: Primary: Percentage of Sites With Reduction in Door to Balloon Time — 83; 50 percentage of sites with improved D2B
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Non Intervention (Other); Agressive Intervention Process Improvement Strategies (Other)
- Age
- Pediatric, Adult, Older Adult
- Sex
- All
- Sponsor
- University of Michigan
- Primary completion
- Feb 2006
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Percentage of Sites With Reduction in Door to Balloon Time |
83; 50 | — |
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.
Eligibility Criteria
Inclusion Criteria
- Acute ST segment myocardial infarction, non transfer patients, with symptom onset to balloon time less than or equal to 24 hours.
Exclusion Criteria
- Patients transferred from one facility to another,
- non ST segment myocardial infarction patients.
Data sourced from ClinicalTrials.gov (NCT01625104). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.