Protocol v28.0 30/06/2025 Rotherham Principal Investigator: Professor Anil Hormis Research team member: Dr Katie Webb
research topic:
Dexamethasone in community acquired pnuemonia.
trial groups:
Intervention: 6mg dexamethasone for 10 days or until discharged, whichever is soonest Control: Usual care
inclusion criteria:
>18 years old, hospitilised with Community-acquired pneumonia (CAP) with planned antibiotic treatment (excluding patients with suspected or confirmed SARS-CoV-2, influenza, active pulmonary tuberculosis or Pneumocystis jirovecii pneumonia) - symptoms of LRTI and radiological evidence
No medical history that might, in the opinion of the attending clinician, put the patient at significant risk if he/she were to participate in the trial
exclusion criteria:
Condition explained by alternative diagnoses e.g. heart failure
Pregnancy and breast feeding
Consideration of important side effects e.g. risk of hyperglycaemia (QDS BMs), peptic ulceration, psychiatric reactions, fluid retention, risk of adrenal insufficiency
Confirmed COVID, influenza, PCP, active TB
consent:
Formal consent is required for RECOVERY trial enrolment/randomisation. If you think your patient is in any way eligible please contact the research team who will review the full inclusion/exclusion criteria and approach for consent.