NCT00794001Recruiting
Feedback Intervention and Treatment Times in ST- Elevation Myocardial Infarction
Feedback Intervention and Treatment Times in ST- Elevation Myocardial Infarction (FITT-STEMI): A Multicenter Trial Analyzing the Effects of Systematic Data Feedback on Treatment Quality and Survival Rates.
Source: ClinicalTrials.gov · Last updated 30 Mar 2023 · Not updated for over 12 months - ask the site whether it is still open
Brief summary (registry, in English)
Part I (Pilot Phase): The purpose of this study is to examine if formalized data assessment and systematic feedback improves treatment times (i.e. contact-to-balloon time and door-to-balloon time) in patients with myocardial infarction with ST-segment elevation (STEMI). Part II (Implementation Phase): The Purpose is to prospectively investigate if survival can be improved by stringent use of this concept of formalized data analysis and systematic feedback of procedural and clinical data to all participating physicians and other members of the STEMI patients treating personnel. Part III (Advance Phase): The purpose is to develop, introduce and evaluate prospectively an automated, highly standardized feedback tool informing participating centers on key performance characteristics (procedural and clinical outcomes).
- Status (registry)
- Recruiting
- Study type
- Interventional
- Enrollment
- 50000 (estimated)
- First submitted
- 18 Nov 2008
- Start date
- Oct 2007
- Primary completion date
- Dec 2025
- Lead sponsor
- Karl Heinrich Scholz
- Diseases
- Coronary artery disease
- NCT number
- NCT00794001
What you commit to
- Study type: Interventional
- Planned participants: 50000
- From Oct 2007 to the primary completion date, Dec 2025
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Other
- STEMI-patients with duration of infarct-related symptoms longer than 24 hours are excluded
Who the study is looking for
- all patients who received a diagnosis of STEMI\* and were transported to the cardiac catheterization laboratory of the primary PCI center with the intention to perform primary PCI.
- STEMI definition:
- elevation of the ST-segments of greater than or equal to 0.1 mV in at least two contiguous limb- or precordial leads
- new or presumable new left bundle branch block in the presence of typical symptoms
Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Save your city in your profile to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| St.Bernward Hospital Coordinator of this site? Confirm its status | Hildesheim | Germany | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.