The Pre-hospital Evaluation of Sensitive Troponin (PRESTO) Study

Status Active, not recruiting

Clinical Trial Summary

The aim of the study is to assess whether a decision aid that is currently used in hospitals across Greater Manchester to determine how likely it is that a patient has a serious heart problem is still accurate in the pre-hospital environment.

Clinical Trial Description

The Investigators will aim to recruit up to 700 participants, aged 18-100, who call 999 with a complaint of chest pain and are subsequently attended by the ambulance service. A blood sample will be taken in the ambulance as well as information about the participant's symptoms, past medical history, physical examination findings and heart tracing findings. The participant will then be transferred to hospital, where another blood sample will be taken. Both of these blood samples will be analysed at a later date for the cardiac marker, troponin. Participants will then be followed up after 30 days via screening of their clinical records and contacting their GP. The investigators will gather information on the participant's initial admission to hospital, as well as any further hospital admissions and investigations that have occurred within the 30 days since this admission. The information collected will include data on serial cardiac marker testing; other laboratory analyses; length of stay; all imaging investigations and procedures; and details of any haemorrhagic complications. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT03561051
Study type	Observational
Source	Manchester University NHS Foundation Trust
Contact
Status	Active, not recruiting
Phase
Start date	October 16, 2018
Completion date	January 1, 2025

View Details

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