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Clinical Trials/ACTRN12610000766011
ACTRN12610000766011
Completed
未知

A study to compare the effectiveness, when applied to clinical practice of an ‘accelerated’ chest pain diagnostic pathway, against the standard investigative process for adults presenting with possible cardiac chest pain at Christchurch Hospital.

Canterbury District Health Board0 sites542 target enrollmentSeptember 15, 2010

Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
Canterbury District Health Board
Enrollment
542
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
September 15, 2010
End Date
August 4, 2012
Last Updated
6 years ago
Study Type
Interventional
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • 1\.Adults \> 18 years of age
  • 2\.Presenting acutely to Christchurch hospital ED with chest pain (or discomfort) suggestive of AMI for whom, following initial clinical assessment, the attending clinician(s) intends to perform serial Cardiac Troponin (cTns), as part of the current chest pain investigation pathway for possible AMI.

Exclusion Criteria

  • 1\. ST Segment Elevation Myocardial Infarction (STEMI) present on any ECG.
  • 2\. Aged less than 18 years old
  • 3\. Proven or suspected non\-coronary pathology as the cause of chest pain
  • 4\. Patients who will require admission regardless of a negative cTn, due to other medical conditions, need for other investigations or social considerations.
  • 5\. Transfers from other hospitals
  • 6\. Chest pain episode began over \> 12 hours ago and still persisting pain
  • 7\. Subjects previously enrolled in this study
  • 8\. Patient (or Legal Representative) unable or unwilling to provide informed consent.
  • 9\. Anticipated problem with follow\-up e.g. resident outside New Zealand
  • 10\. Researcher does not feel that recruitment is appropriate (e.g. terminal illness)

Outcomes

Primary Outcomes

Not specified

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