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ASPECT

Aspirin after hospitalisation with Pneumonia to prevent cardiovascular Events randomised Controlled Trial

Pneumonia Adult ≥ 50 years Cardiovascular prevention

Study aim

Looking at whether aspirin can help prevent strokes in patients with pneumonia

Inclusion Criteria

  • Participants aged ≥ 50 years
  • Admitted to hospital with pneumonia, or decision to admit
  • Symptoms and signs of acute lower respiratory tract infection
  • Radiographic changes in keeping with infection on chest radiograph, CT scan, or lung ultrasound scan

Exclusion Criteria

  • Already taking regular prescribed anti-platelet medication, including aspirin, clopidogrel, cangrelor, selexipag, cilostazol, dipyridamole, prasugrel, ticagrelor, abciximab, eptifibatide, tirofiban, epoprostenol, or iloprost
  • Known allergy, previous important adverse reaction, or contraindication to aspirin
  • At high risk of excessive bleeding (e.g. large trauma or haemorrhage, urgent need for major surgery, or uncorrectable coagulopathy) in the opinion of the treating physician
  • Hospital-acquired pneumonia, defined as related to an inpatient hospital stay within the last 10 days, or acquired at least 48 hours after current admission
  • Discharged without a 'Decision to Admit' to hospital by urgent care / emergency department
  • Unlikely to tolerate or adhere to medication regimen
  • Prisoners
  • Known to be pregnant
  • Life expectancy less than 3 months due to pre-existing condition (e.g. terminal malignancy)
  • Presentation more likely due to acute COVID-19 pneumonitis in the opinion of the treating physician — i.e. newly positive PCR or similar antigen test for COVID-19
  • Enrolment onto another study where the combined burden on the participant would be too high, or where dual enrolment would compromise one or both studies' objectives
Note: Anti-coagulation medication is not an exclusion criterion; however, the increased bleeding risk should be considered by the clinician.

Step-by-step recruitment guide

Standard working hours (09:00 – 17:00)
1 Contact the ED Research Team when an eligible patient arrives in the ED — send a message via Epic chat to "ED Research Team" or phone 217907.
2 The ED Research Team will see the patient to arrange consent and randomisation.
Out of hours & weekends
1 Send the ED Research Team an Epic message with the patient's details. The team has 7 days from admission to approach the patient to discuss the trial.

Equipment & materials locations

Ambulatory bay rack Reception box ED Research cupboard

Further information