- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01197716
German Chest Pain Unit (CPU)-Register
Deutsches CPU-Register. Unterstützt Durch Die Deutsche Gesellschaft für Kardiologie.
Study Overview
Status
Conditions
Detailed Description
The aim of a Chest Pain Unit (CPU) is to clarify unclear chest pain quickly and specifically. Present data from Germany, the USA and England prove that the organisation models of a CPU lead beside a drastic reduction of mortality also to a cost reduction as well as a shortening of the average inpatient hospital stays.
Therefore it seems reasonable to assign a minimum standard to CPUs. Although there are internationally already standards for CPUs up to complete certification programmes, it is an explicit wish of the German society for cardiology (DGK) to create an own standard which considers on the national circumstances.
The aim of the CPU register is the internal and external validation of the care quality of CPU including Benchmark reports and risk-adjusted comparisons.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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-
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Frankfurt/Main, Germany
- Bethanien Krankenhaus
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
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).
Study Plan
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Prospective
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Internal and external validation of the medical care quality in the field of Chest Pain Units
Time Frame: hospital stay
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including benchmark reports and risk adjusted comparisons.
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hospital stay
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Documentation of CPU complications
Time Frame: up to 30 hours on average
|
including mortality, serious but non-fatal complications (e.g.
stroke, heavy and moderate bleedings) as well as documentation of the medication at hospital discharge
|
up to 30 hours on average
|
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Documentation of long-term mortality and serious but non-fatal complications
Time Frame: 3 months after discharge
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as well as additional hospital admissions and medication
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3 months after discharge
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Collaborators and Investigators
Investigators
- Study Chair: Harald Darius, MD, Vivantes Clinic Neukölln
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- German CPU-Register
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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