Skip to main content
Clinical Trials/NCT01197716
NCT01197716
Completed
Not Applicable

Deutsches CPU-Register. Unterstützt Durch Die Deutsche Gesellschaft für Kardiologie.

Stiftung Institut fuer Herzinfarktforschung1 site in 1 country34,470 target enrollmentDecember 2008
ConditionsChest Pain

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Chest Pain
Sponsor
Stiftung Institut fuer Herzinfarktforschung
Enrollment
34470
Locations
1
Primary Endpoint
Internal and external validation of the medical care quality in the field of Chest Pain Units
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

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.

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.

Registry
clinicaltrials.gov
Start Date
December 2008
End Date
December 2015
Last Updated
9 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Stiftung Institut fuer Herzinfarktforschung
Responsible Party
Sponsor

Eligibility 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).

Outcomes

Primary Outcomes

Internal and external validation of the medical care quality in the field of Chest Pain Units

Time Frame: hospital stay

including benchmark reports and risk adjusted comparisons.

Secondary Outcomes

  • Documentation of CPU complications(up to 30 hours on average)
  • Documentation of long-term mortality and serious but non-fatal complications(3 months after discharge)

Study Sites (1)

Loading locations...

Similar Trials