Pneumonia Clinical Trials

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Randomised Evaluation of COVID-19 Therapy

Who is this study for? Children with PIMS-TS (hyper-inflammatory state associated with COVID-19)
Status: Recruiting
Location: See all (16) locations...
Intervention Type: Drug, Biological
Study Type: Interventional
Study Phase: Phase 3
SUMMARY

RECOVERY is a randomised trial of treatments to prevent death in patients hospitalised with pneumonia. The treatments being investigated are: COVID-19: Lopinavir-Ritonavir, Hydroxychloroquine, Corticosteroids, Azithromycin, Colchicine, IV Immunoglobulin (children only), Convalescent plasma, Casirivimab+Imdevimab, Tocilizumab, Aspirin, Baricitinib, Empagliflozin, Sotrovimab, Molnupiravir, Paxlovid or Anakinra (children only) Influenza: Baloxavir marboxil, Oseltamivir, Corticosteroids (dexamethasone) Community-acquired pneumonia: Corticosteroids (dexamethasone)

Eligibility
Participation Requirements
Sex: All
Healthy Volunteers: f
View:

⁃ Eligibility Criteria (as per Protocol v28.0):

⁃ Patients are eligible for the study if all of the following are true:

⁃ (i) Hospitalised

⁃ (ii) Pneumonia syndrome

⁃ In general, pneumonia should be suspected when a patient presents with:

• typical symptoms of a new respiratory tract infection (e.g. influenza-like illness with fever and muscle pain, or respiratory illness with cough and shortness of breath); and

• objective evidence of acute lung disease (e.g. consolidation or ground-glass shadowing on X-ray or CT, hypoxia, or compatible clinical examination); and

• alternative causes have been considered unlikely or excluded (e.g. heart failure).

⁃ However, the diagnosis remains a clinical one based on the opinion of the managing doctor (the above criteria are just a guide).

⁃ (iii) One of the following diagnoses:

• Confirmed influenza A or B infection (including patients with SARS-CoV-2 co-infection)

• 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)

⁃ (iv) 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

⁃ Patients with suspected or confirmed active pulmonary tuberculosis or Pneumocystis jirovecii pneumonia (also known as PCP or PJP) are excluded from the CAP comparison, as these infections are caused by specific organisms with distinct pathologies, and so are not usually categorised as CAP. Eligibility for the CAP comparison also requires planned antibiotic treatment, so patients being treated solely for fungal or viral pneumonia are not eligible.

⁃ Patients with SARS-CoV-2 and influenza co-infection are eligible, but would be excluded from certain comparisons if the attending clinician believes that there is a specific contra-indication to one of the active drug treatment arms (see Protocol Appendix 2, Appendix 3 for children, and Appendix 4 for pregnant and breastfeeding women), or that the patient should definitely be receiving one of the active drug treatment arms then that arm will not be available for randomisation for that patient. For patients who lack capacity, an advanced directive or behaviour that clearly indicates that they would not wish to participate in the trial would be considered sufficient reason to exclude them from the trial.

⁃ Patients who have been previously recruited into RECOVERY are eligible to be recruited again as long as their previous randomisation was \>6 months ago. Patients will not be recruited into the same randomised comparison (e.g. sotrovimab vs. usual care) on more than one occasion, regardless of how far apart they occur.

⁃ In some locations, children (aged \<18 years) will not be recruited, to comply with local and national regulatory approvals (see Appendix 6).

⁃ Note: the eligibility criteria has changed from COVID-19 to pneumonia (Influenza \& CAP). For detailed information about previous eligibility criteria please see the previous Protocol's on the study website: https://www.recoverytrial.net/uk/for-site-staff/site-set-up-1/regulatory-documents

Locations
Other Locations
Belgium
Belgian sites are managed by the European Clinical Research Alliance on Infectious Diseases
RECRUITING
Brussels
Estonia
Estonian sites are managed by the European Clinical Research Alliance on Infectious Diseases
RECRUITING
Tallinn
France
French sites are managed by the European Clinical Research Alliance on Infectious Diseases
RECRUITING
Paris
Ghana
Kumasi Center for Collaborative Research in Tropical Medicine KNUST
RECRUITING
Kumasi
India
Indian Council of Medical Research, Division of Epidemiology and Communicable Diseases
COMPLETED
New Delhi
Indonesia
Eijkman Oxford Clinical Research Unit (EOCRU), Eijkman Institute for Molecular Biology
RECRUITING
Jakarta
Italy
Italian sites are managed by the European Clinical Research Alliance on Infectious Diseases
RECRUITING
Roma
Nepal
Clinical Trial Unit, Oxford University Clinical Research Unit-Nepal, Patan Academy of Health Sciences
RECRUITING
Kathmandu
Netherlands
Dutch sites are managed by the European Clinical Research Alliance on Infectious Diseases
RECRUITING
Utrecht
Portugal
Portuguese sites are managed by the European Clinical Research Alliance on Infectious Diseases
RECRUITING
Lisbon
Romania
Romanian sites are managed by the European Clinical Research Alliance on Infectious Diseases
RECRUITING
Bucharest
South Africa
Wits Health Consortium
RECRUITING
Johannesburg
Spain
Spanish sites are managed by the European Clinical Research Alliance on Infectious Diseases
RECRUITING
Barcelona
Sweden
Swedish sites are managed by the European Clinical Research Alliance on Infectious Diseases
RECRUITING
Stockholm
United Kingdom
Nuffield Department of Population Health, University of Oxford
RECRUITING
Oxford
Viet Nam
Oxford University Clinical Research Unit, Centre for Tropical Medicine
RECRUITING
Ho Chi Minh City
Contact Information
Primary
Leon Peto
recoverytrial@ndph.ox.ac.uk
+44 (0)1865 743743
Time Frame
Start Date: 2020-03-19
Estimated Completion Date: 2038-09-30
Participants
Target number of participants: 70000
Treatments
No_intervention: Standard Care
Patient receives usual hospital care
Active_comparator: Corticosteroids
First (main) randomisation part A (COVID-19)~\[This arm is now closed to recruitment\]
Active_comparator: Hydroxychloroquine
First (main) randomisation part A (COVID-19)~\[This arm is now closed to recruitment\]
Active_comparator: Lopinavir-Ritonavir
First (main) randomisation part A (COVID-19)~\[This arm is now closed to recruitment\]
Active_comparator: Azithromycin
First (main) randomisation part A (COVID-19)~\[This arm is now closed to recruitment\]
Active_comparator: Convalescent plasma
First (main) randomisation part B (COVID-19)~\[This arm is now closed to recruitment\]
Active_comparator: Tocilizumab
Participants with progressive COVID-19 (as evidenced by hypoxia and an inflammatory state) may undergo randomisation between Tocilizumab and no additional treatment.~(Children with COVID-19 pneumonia are not eligible for this comparison).~\[This arm is now closed to recruitment\]
Active_comparator: Intravenous Immunoglobulin
First (main) randomisation part A (children only)~\[This arm is now closed to recruitment\]
Active_comparator: Synthetic neutralising antibodies
First (main) randomisation part B (COVID-19)~\[This arm is now closed to recruitment\]
Active_comparator: Aspirin
First (main) randomisation part C (COVID-19)~\[This arm is now closed to recruitment\]
Active_comparator: Colchicine
First (main) randomisation part A (COVID-19)~\[This arm is now closed to recruitment\]
Active_comparator: Baricitinib
First (main) randomisation part D (COVID-19)~\[This arm is now closed to recruitment\]
Active_comparator: Anakinra
Randomisation for children only with PIMS-TS~(Children with COVID-19 pneumonia are not eligible for this comparison).~\[This arm is now closed to recruitment\]
Active_comparator: Dimethyl fumarate
First (main) randomisation part A (COVID-19) (UK adults only; early phase assessment)~\[This arm is now closed to recruitment\]
Active_comparator: High Dose Corticosteroids
First (main) randomisation part E (COVID-19)~\[This arm is now closed to recruitment\]
Active_comparator: Empagliflozin
First (main) randomisation part F (COVID-19)~\[This arm is now closed to recruitment\]
Active_comparator: Sotrovimab
First (main) randomisation part J (COVID-19)~\[This arm is now closed to recruitment\]
Active_comparator: Molnupiravir
First (main) randomisation part K (COVID-19)~\[This arm is now closed to recruitment\]
Active_comparator: Paxlovid
First (main) randomisation part L (COVID-19)~\[This arm is now closed to recruitment\]
Active_comparator: Baloxavir marboxil
Randomisation part G (influenza)
Active_comparator: Oseltamivir
Randomisation part H (influenza)
Active_comparator: Corticosteroids (dexamethasone) (influenza arm)
Randomisation part I (influenza)
Active_comparator: Corticosteroids (dexamethasone) (community-acquired pneumonia arm)
Randomisation part M (community-acquired pneumonia)
Sponsors
Collaborators: UK Research and Innovation, Bill and Melinda Gates Foundation, Wellcome Trust, Medical Research Council Population Health Research Unit, Health Data Research UK, NIHR Health Protection Research Unit in Emerging and Zoonotic Infections, Flu Lab, Department for International Development, United Kingdom, National Institute for Health Research, United Kingdom
Leads: University of Oxford

This content was sourced from clinicaltrials.gov