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Feedback Intervention and Treatment Times in ST- Elevation Myocardial Infarction

NCT00794001 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 50000

Last updated 2023-03-30

No results posted yet for this study

Summary

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).

Conditions

Interventions

BEHAVIORAL

Data analysis and Feedback

Data analysis feedback: quarterly meetings with all stakeholders to present data and discuss potential areas of improvement.

Sponsors & Collaborators

  • ALKK: Arbeitsgemeinschaft Leitender Kardiologischer Krankenhausaerzte

    collaborator UNKNOWN

  • The German Heart Foundation

    collaborator OTHER

  • Aerztekammer Niedersachsen

    collaborator UNKNOWN

  • Karl Heinrich Scholz

    lead OTHER

Principal Investigators

  • Karl H. Scholz, MD. · St.Bernward Hospital

Study Design

Allocation
NA
Purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2007-10-31
Primary Completion
2025-12-31
Completion
2026-12-31

Countries

  • Germany

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00794001 on ClinicalTrials.gov