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
Sponsor:
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
  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
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

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 October 20, 2014