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OPTAMI (Optimized Therapy of Acute Myocardial Infarction) - Registry

OPTAMI (Optimierte Therapie Des Akuten Myokard-Infarktes) - Register

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01197729
Acronym
OPTAMI
Enrollment
3248
Registered
2010-09-09
Start date
2005-10-31
Completion date
2010-02-28
Last updated
2024-12-20

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

Conditions

Myocardial Infarction, Non-ST-Elevation Myocardial Infarction, ST-Elevation Myocardial Infarction

Keywords

Myocardial infarction, ST-Elevation myocardial infarction, Non-ST-Elevation myocardial infarction, Register, CARDS

Brief summary

OPTAMI documents the characteristics of consecutive patients with acute STEMI and NSTEMI in hospital everyday-life in Germany, their acute and adjuvant medication treatment, events until discharge (e.g. mortality, stroke, re-MI), and their medication for secondary prevention at discharge. In the follow up-period of one year, information is collected concerning events as mortality, stroke, re-MI, coronary interventions (PCI, CABG) and re-hospitalisation. The implementation of guideline-adjusted therapy in hospital everyday-life is reviewed. The usefulness of the European standard for data acquisition in cardiology (CARDS = Cardiology Audit and Registration Standards) is evaluated.

Interventions

None listed

Sponsors

Klinikum Nürnberg
CollaboratorOTHER
University Hospital Muenster
CollaboratorOTHER
GlaxoSmithKline
CollaboratorINDUSTRY
Stiftung Institut fuer Herzinfarktforschung
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* all patients admitted to hospital with an acute ST-Elevation myocardial infarction or with an acute Non-ST-Elevation myocardial infarction, both not older than 24 h

Exclusion criteria

* missing informed consent

Design outcomes

Primary

MeasureTime frame
Documentation of characteristics from consecutive patients with an acute STEMI or an acute NSTEMI in hospital daily routine in Germany.10/01/2005-02/01/2009

Secondary

MeasureTime frame
Documentation of hospital mortality and non-fatal cerebrovascular complications (stroke, re-myocardial infarction)10/01/2005-02/01/2009
Documentation of medication for secondary prevention at hospital discharge10/01/2005-02/01/2009
Documentation of acute invasive and adjuvant medical therapy of STEMI and NSTEMI in hospital daily routine in Germany10/01/2005-02/01/2009
Verification of the benefits of the European Standards for Data Collection for Cardiology (CARDS = Cardiology Audit and Register Standards) in daily hospital routine.10/01/2005-02/01/2009
Verification of the implementation of therapy according to the guidelines for STEMI and NSTEMI patients in daily hospital routine in Germany.10/01/2005-02/01/2009
Documentation of the one-year mortality, the non-fatal cerebrovascular complications (stroke, re-myocardial infarction) as well as of the coronar interventions (PCI, Bypass operation) and hospital admissions during the first year post STEMI or NSTEMI10/01/2005-02/01/2009

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026