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Infarction Register (ADMIRE)

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT00763945
Recruitment Status : Completed
First Posted : October 1, 2008
Last Update Posted : September 18, 2009
Sponsor:
Information provided by:
RWTH Aachen University

Brief Summary:
The Aachener Digitale Myokardinfarkt Register (ADMIRE) is a prospektive registry study which was designed in order to obtain data of patients with acute coronary syndrome and herewith control and optimize guideline conform therapy of these patients.

Condition or disease Intervention/treatment
Acute Coronary Syndrome Other: data collection

Detailed Description:

Aims of this registry stdy are

documentation of the characteristics of all patients representing to the RWTH Aachen University Hospital (UKA) with STEMI or NSTEMI documentation of the invasive and adjuvant medicinal therapy of STEMI and NSTEMI at UKA documentation of the in-hospital mortality documentation of the procedure-associated complications documentation of therapeutic principals for patients with STEMI or NSTEMI at UKA and investigation conformity of treatment with already established guidelines

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Study Type : Observational
Estimated Enrollment : 5000 participants
Time Perspective: Prospective
Official Title: Aachen Digital Myocardial Infarction Register
Study Start Date : March 2006
Actual Primary Completion Date : March 2009
Actual Study Completion Date : March 2009

Group/Cohort Intervention/treatment
1
Patients representing to the hospital with acute coronary syndrome
Other: data collection
The data of patients is collected from their hospital documentation The follow-up of all patients is done via phone calls in order to collect data about the outcome of each patient





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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
Patients who present to the hospital with acute coronary syndrome
Criteria

Inclusion Criteria:

  • acute coronary syndrome

Exclusion Criteria:

  • under age or not able to give informed consent

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00763945


Locations
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Germany
Department of Medicine, Division of Cardiology, Pulmonary Diseases and Vascular Medicine at the University Hospital, RWTH Aachen
Aachen, NRW, Germany, 52074
Sponsors and Collaborators
RWTH Aachen University
Investigators
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Study Director: Verena Deserno, M.Sc. Medical Faculty of the RWTH Aachen University
Principal Investigator: Rainer Hoffmann, MD, Ph.D. RWTH Aachen University Hospital
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Responsible Party: PD Dr. med. Wolfgang Lepper, RWTH Aachen University, Medical Faculty
ClinicalTrials.gov Identifier: NCT00763945    
Other Study ID Numbers: ADMIRE
First Posted: October 1, 2008    Key Record Dates
Last Update Posted: September 18, 2009
Last Verified: September 2009
Keywords provided by RWTH Aachen University:
Acute coronary Syndrome
STEMI
NSTEMI
Registry
Additional relevant MeSH terms:
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Acute Coronary Syndrome
Infarction
Pathologic Processes
Ischemia
Necrosis
Myocardial Ischemia
Heart Diseases
Cardiovascular Diseases
Vascular Diseases