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)
Investigators
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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