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Completed

NCT Number: NCT02693015

Impact of Time to Coronary Angiography on Survival for NSTEMI

This study aims to investigate the extent to which the time to angiography impacts on survival in patients hospitalised with NSTEMI.

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Key information

About this study

The use of an invasive strategy for the management of NSTEMI according to estimated risk of 6 month mortality is recommended by international guidelines. NSTEMI appropriate for coronary angiography (and percutaneous intervention) have better outcomes compare with NSTEMI who are medically managed. Whilst the national and international guidelines recommend that the timing of (in-hospital) coronary angiography (<24, 24-72, 72-96 and <96 hours) is based upon estimated clinical risk (using the GRACE risk score) there is scientific and clinical uncertainty as to the incremental benefit that more urgent invasive treatments strategies have over and above that of delayed strategies. Moreover, the investigators recent research has shown that in the UK, may NSTEMI (eligible) for coronary angiography fail to achieve care according to the recommended time thresholds, and this is associated with potentially avoidable premature death.

This study aims to investigate the extent to which the time to angiography impacts on survival in patients hospitalised with NSTEMI. It will characterise patients according to their estimated risk of death, their time to angiography, and associated outcomes. The investigators anticipate that this observational study will provide Level B evidence for the benefits of the timing of an invasive strategy according to the GRACE risk score. The investigators are aware that the NICE guidelines for the management of acute chest pain are to be updated in 2016.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • The target population will be all patients aged 18 to 100 years recorded within MINAP from 2004 to 2013 who have been hospitalised with NSTEMI and received coronary angiography.

Exclusion criteria

  • Age below 18 or above 100 or age missing
  • Diagnosis not NSTEMI
  • Patients who did not receive coronary angiography - as this is the investigators explanatory variable

Treatment and study plan

Primary outcomes

  1. All-cause mortality

    Time frame: 30-day mortality since hospitalisation

  2. Mortality

    Time frame: 1-year mortality since hospitalisation

Sponsors and collaborators

Lead sponsor

University of Leeds

Other

Registry information

Official study title

Impact of Time to Coronary Angiography on Survival for NSTEMI: an Observation Study Using a Nationwide Registry

Important dates

Study start
2004
Primary completion
2013
Study completion
2013
First posted
Feb 26, 2016
Registry last updated
Feb 26, 2016

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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