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Clinical Trials/ISRCTN86184521
ISRCTN86184521
Completed
未知

Randomised controlled trial of the LoDED (Limit of Detection of Troponin and ECG Discharge) strategy versus usual care in adult chest pain patients attending the Emergency Department

orth Bristol NHS Trust0 sites632 target enrollmentApril 23, 2018

Overview

Phase
未知
Intervention
Not specified
Conditions
Chest pain
Sponsor
orth Bristol NHS Trust
Enrollment
632
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

2020 Results article in https://pubmed.ncbi.nlm.nih.gov/32371401/ results (added 21/05/2020) 2018 Protocol article in https://pubmed.ncbi.nlm.nih.gov/30282688/ (added 17/08/2022) 2020 Results article in https://pubmed.ncbi.nlm.nih.gov/33298603/ Patients' and health professionals' perceptions (added 31/08/2023)

Registry
who.int
Start Date
April 23, 2018
End Date
April 3, 2019
Last Updated
2 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
orth Bristol NHS Trust

Eligibility Criteria

Inclusion Criteria

  • 1\. Age \=18 years
  • 2\. Presenting to ED with chest pain and triggering the chest pain investigation pathway i.e. treating clinician intends to perform investigation to rule out a cardiac cause
  • 3\. Peak symptoms occurred \<6 hours prior to presentation to the ED

Exclusion Criteria

  • 1\. ST\-elevation myocardial infarction or ischaemic ECG (new T wave inversion \> 3mm or ST depression \> 1mm) as judged by the treating clinician
  • 2\. Clear non\-ACS cause for chest pain found at presentation (e.g. pulmonary embolism, pneumonia, aortic dissection)
  • 3\. Initial hs\-troponin result known to the treating clinician
  • 4\. Hospital admission indicated due to other medical/social reasons
  • 5\. Chest pain due to arrhythmia (new\-onset atrial fibrillation, atrial flutter, sustained supraventricular tachycardia, second\-degree or complete heart block, or sustained or recurrent ventricular arrhythmias)
  • 6\. Unable to provide written informed consent (lacks capacity)
  • 7\. Unwilling to provide written informed consent
  • 8\. Pain too severe to provide written informed consent
  • 9\. Follow\-up will be impossible i.e. lives abroad or no fixed abode
  • 10\. Previous inclusion in the study

Outcomes

Primary Outcomes

Not specified

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