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AMIS Plus - National Registry of Acute Myocardial Infarction in Switzerland

National Registry of Acute Myocardial Infarction in Switzerland

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01305785
Acronym
AMIS Plus
Enrollment
60000
Registered
2011-03-01
Start date
1997-01-31
Completion date
Unknown
Last updated
2013-04-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Coronary Syndrome

Brief 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.

Detailed description

The AMIS Plus project has two main goals: 1. To Maintain a Nationwide Registry * An ongoing nationwide registry (databank) of acute coronary syndromes * Description of the patient population with acute coronary syndromes * Description of characteristics of treatment and hospitalization * Description of outcomes 3- and 12-months after admission for ACS * Epidemiological studies, e.g. definition of risk factors of patients with acute coronary syndromes, hospital mortality, time and cost-effective strategies as well as outcome measures 2. Quality Control * Evaluation of compliance with guidelines for the medical care of acute coronary syndromes * Internal quality control through regular feedback and benchmarking Methods All Swiss hospitals admitting patients with acute coronary syndrome are eligible. Data are collected on demographics, risk factors, symptoms, laboratory results, invasive therapy, complications and medication. Since the start in January 1997, the method of data collection has continuously improved in order to suit the different needs and technological advancements of the participating hospitals. Participants can either complete paper questionnaires and send them directly to the AMIS Plus Data Center at the Institute of Social and Preventive Medicine in Zurich where these questionnaires are then checked and entered online or they can enter data directly online (AMIS online questionnaire). Data security has a high priority. Participant identification (code for hospital and physician) and a password are required to access the data entry form and send data.

Interventions

None listed

Sponsors

University of Zurich
CollaboratorOTHER
University Hospital, Geneva
CollaboratorOTHER
Insel Gruppe AG, University Hospital Bern
CollaboratorOTHER
University Hospital, Basel, Switzerland
CollaboratorOTHER
Triemli Hospital
CollaboratorOTHER
Kantonsspital Baden
CollaboratorOTHER
Cantonal Hospital of St. Gallen
CollaboratorOTHER
University Hospital Freiburg
CollaboratorOTHER
Cantonal Hospital, Frauenfeld
CollaboratorOTHER
Hospital Centre Biel/Bienne
CollaboratorOTHER
Spital Lachen AG
CollaboratorOTHER
Cardiocentro Ticino
CollaboratorOTHER
Luzerner Kantonsspital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

Patients who had symptoms within the last 48 hours at hospital admission with a discharge clinical diagnosis of acute myocardial infarction or patients who suffered an acute myocardial infarction in hospital during a hospitalization for other reasons.

Exclusion criteria

Since January 2012, patients with unstable angina are no longer included.

Countries

Switzerland

Contacts

Primary ContactPaul Erne, MD
Paul.Erne@luks.ch++41 41 205 51 06

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 22, 2026