AMIS Plus - National Registry of Acute Myocardial Infarction in

Status Recruiting

Clinical Trial 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.

Clinical Trial 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. ;

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT01305785
Study type	Observational
Source	Luzerner Kantonsspital
Contact	Paul Erne, MD
Phone	++41 41 205 51 06
Email	Paul.Erne@luks.ch
Status	Recruiting
Phase	N/A
Start date	January 1997

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Clinical trials are conducted in a series of steps, called phases - each phase is designed to answer a separate research question.

Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.

AMIS Plus - National Registry of Acute Myocardial Infarction in Switzerland — AMIS Plus

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms