Last updated: May 16, 2022
Sponsor: University of Trieste
Overall Status: Completed
Phase
3
Condition
Respiratory Syncytial Virus (Rsv) Infection
Pneumonia
Covid-19
Treatment
N/AClinical Study ID
NCT04636671
MEDEAS1
Ages > 18 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- Able to understand and sign the informed consent
- SARS-CoV-2 positive on at least one upper respiratory swab or bronchoalveolar lavage
- PaO2 <= 60 mmHg or SpO2 <= 90% or on oxygen therapy (any), CPAP or NPPV atrandomization
- Age >= 18 years old at randomization
Exclusion
Exclusion Criteria:
- On invasive mechanical ventilation (either intubated or tracheostomized)
- Heart failure as the main cause of acute respiratory failure
- On long-term oxygen or home mechanical ventilation
- Decompensated liver cirrhosis
- Immunosuppression (i.e., cancer on treatment, post-organ transplantation,HIV-positive, on immunosuppressant therapy)
- On chronic steroid therapy or other immunomodulant therapy (e.g., azathioprine,methotrexate, mycophenolate, convalescent/hyperimmune plasma)
- Chronic renal failure with dialysis dependence
- Progressive neuro-muscular disorders
- Cognitively impaired, dementia or decompensated psychiatric disorder
- Quadriplegia/Hemiplegia or quadriparesis/hemiparesis
- Do-not-resuscitate order
- Participating in other clinical trial including experimental compound with proved orexpected activity against SARS-CoV-2 infection
- Any other condition that in the opinion of the investigator may significantly impactwith patient's capability to comply with protocol intervention
- Refuse to participate in the study or absence of signed informed consent form.
Study Design
Total Participants: 690
Study Start date:
April 14, 2021
Estimated Completion Date:
May 04, 2022
Connect with a study center
Marco Confalonieri
Trieste, TS 34149
ItalySite Not Available


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