German Chest Pain Unit (CPU)-Register
Deutsches CPU-Register. Unterstützt Durch Die Deutsche Gesellschaft für Kardiologie.
1 other identifier
observational
34,470
1 country
1
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Dec 2008
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
December 1, 2008
CompletedFirst Submitted
Initial submission to the registry
September 7, 2010
CompletedFirst Posted
Study publicly available on registry
September 9, 2010
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2015
CompletedStudy Completion
Last participant's last visit for all outcomes
December 1, 2015
CompletedJune 24, 2016
June 1, 2016
7 years
September 7, 2010
June 23, 2016
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Internal and external validation of the medical care quality in the field of Chest Pain Units
including benchmark reports and risk adjusted comparisons.
hospital stay
Secondary Outcomes (2)
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
Eligibility Criteria
Patients admitted to a chest pain unit in a primary care clinic
You may qualify if:
- All patients that are admitted to a Chest Pain Unit are included in this register.
You may not qualify if:
- 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).
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Bethanien Krankenhaus
Frankfurt am Main, Germany
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY CHAIR
Harald Darius, MD
Vivantes Clinic Neukölln
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
September 7, 2010
First Posted
September 9, 2010
Study Start
December 1, 2008
Primary Completion
December 1, 2015
Study Completion
December 1, 2015
Last Updated
June 24, 2016
Record last verified: 2016-06
Data Sharing
- IPD Sharing
- Will not share