German Chest Pain Unit (CPU)-Register
The recruitment status of this study is unknown because the information has not been verified recently.
Verified September 2010 by Stiftung Institut fuer Herzinfarktforschung.
Recruitment status was Recruiting
Recruitment status was Recruiting
Sponsor:
Stiftung Institut fuer Herzinfarktforschung
Information provided by:
Stiftung Institut fuer Herzinfarktforschung
ClinicalTrials.gov Identifier:
NCT01197716
First received: September 7, 2010
Last updated: September 8, 2010
Last verified: September 2010
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Purpose
The Chest Pain Unit (CPU) register is a nationwide scientific investigation, in which data concerning the hospital-stay within the Chest Pain Unit are documented. Furthermore, a Follow-up via telephone is conducted after 3 months.
| Condition |
|---|
|
Chest Pain |
| Study Type: | Observational |
| Study Design: | Observational Model: Cohort Time Perspective: Prospective |
| Official Title: | Deutsches CPU-Register. Unterstützt Durch Die Deutsche Gesellschaft für Kardiologie. |
Resource links provided by NLM:
Further study details as provided by Stiftung Institut fuer Herzinfarktforschung:
Secondary Outcome Measures:
- Internal and external validation of the medical care quality in the field of Chest Pain Units, including benchmark reports and risk adjusted comparisons. [ Time Frame: 12/01/2008 ] [ Designated as safety issue: No ]
- Documentation of CPU complications including mortality, serious but not fatal complications (e.g. stroke, heavy and moderate bleedings etc) as well as documentation of medication at hospital discharge. [ Time Frame: 12/01/2008 ] [ Designated as safety issue: No ]
- Documentation of long-term mortality and serious but non-fatal complication (SCI, stroke, TIA, heavy bleeding etc.) as well as hospital admissions and medication after 3 months. [ Time Frame: 03/01/2009 ] [ Designated as safety issue: No ]
| Estimated Enrollment: | 25000 |
| Study Start Date: | December 2008 |
Eligibility| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
| Sampling Method: | Non-Probability Sample |
Study Population
Patients admitted to a chest pain unit in a primary care clinic
Criteria
Inclusion Criteria:
All patients that are admitted to a Chest Pain Unit are included in this register.
Exclusion Criteria:
Missing informed consent (informed consent can NOT be given in the acute phase of the disease, if consciousness is limited at that time; instead the patient will be asked for his consent at a later point of time, when he is fully conscious).
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01197716
Contacts
| Contact: Jochen Senges, MD | +49-621-5032801 | senges@herzinfarktforschung.de |
Locations
| Germany | |
| Bethanien Krankenhaus | Recruiting |
| Frankfurt/Main, Germany | |
Sponsors and Collaborators
Stiftung Institut fuer Herzinfarktforschung
Investigators
| Study Chair: | Harald Darius, MD | Vivantes Klinikum Neukölln |
More Information
No publications provided
| Responsible Party: | Jochen Senges, MD, Stiftung Institut fuer Herzinfarktforschung (Foundation for Cardiac Infarction Research) |
| ClinicalTrials.gov Identifier: | NCT01197716 History of Changes |
| Other Study ID Numbers: | German CPU-Register |
| Study First Received: | September 7, 2010 |
| Last Updated: | September 8, 2010 |
| Health Authority: | Germany: Ethics Commission |
Keywords provided by Stiftung Institut fuer Herzinfarktforschung:
|
Chest Pain Unit Myocardial infarction Register Admission to a Chest Pain Unit for any reason |
Additional relevant MeSH terms:
|
Chest Pain Pain Signs and Symptoms |
ClinicalTrials.gov processed this record on May 22, 2013