MedTrace Logo

AMIS Plus - National Registry of Acute Myocardial Infarction in Switzerland

NCT01305785 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 60000

Last updated 2013-04-17

No results posted yet for this study

Summary

The AMIS Plus national registry collects and analyzes data on patients with acute myocardial infarction in Switzerland in the pre-admission, hospital and follow-up phases. Emphasis is placed on the evaluation of risk factors, diagnostics, urgent therapy strategies and treatment of acute coronary syndrome. The AMIS Plus data gathered are important for assessing guidelines, improving compliance with guidelines in clinical practice, investigating patient groups not extensively studied in large randomized trials, quality assurance as well as the continuous improvement of therapeutic strategies based on a large database.

Conditions

  • Acute Coronary Syndrome

Sponsors & Collaborators

  • University of Zurich

    collaborator OTHER

  • University Hospital, Geneva

    collaborator OTHER

  • Insel Gruppe AG, University Hospital Bern

    collaborator OTHER

  • University Hospital, Basel, Switzerland

    collaborator OTHER

  • Triemli Hospital

    collaborator OTHER

  • Kantonsspital Baden

    collaborator OTHER

  • Cantonal Hospital of St. Gallen

    collaborator OTHER

  • University Hospital Freiburg

    collaborator OTHER

  • Cantonal Hospital, Frauenfeld

    collaborator OTHER

  • Hospital Centre Biel/Bienne

    collaborator OTHER

  • Spital Lachen AG

    collaborator OTHER

  • Cardiocentro Ticino

    collaborator OTHER

  • Luzerner Kantonsspital

    lead OTHER

Principal Investigators

  • Paul Erne, MD · AMIS Plus Data Center

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
1997-01-31

Countries

  • Switzerland

Study Locations

More Related Trials

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 NCT01305785 on ClinicalTrials.gov