Phase
Condition
Respiratory Syncytial Virus (Rsv) Infection
Pregnancy Complications
Pneumonia
Treatment
N/AClinical Study ID
Female
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria: Participants eligible for inclusion in this Trial must meet all of the following criteria: Voluntary written informed consent of the participant or their legally authorizedrepresentative obtained prior to any screening procedures Pregnant patients admitted to the Hospital during the COVID-19 pandemic:
Patients with confirmed COVID-19 infection (see below)
Symptomatic patients suspicious for COVID-19 infection (swab is taken on admission)
Patients asymptomatic for COVID19 with other feto-maternal diseases or who come fordelivery or caesarean section All participants that are considered for Trial participation, per the above criteria willbe documented on the Screening Log, including Screen Failures. Definition of suspected case (WHO guideline, ISUOG)
A patient with acute respiratory illness (fever and at least one sign/symptom ofrespiratory disease (e.g. cough, shortness of breath)) AND with no other etiology thatfully explains the clinical presentation AND a history of travel to or residence in acountry/area or territory reporting local transmission of COVID-19 infection duringthe 14 days prior to symptom onset; OR
A patient with any acute respiratory illness AND who has been in contact with aconfirmed or probable case of COVID-19 infection in the 14 days prior to onset ofsymptoms; OR
A patient with severe acute respiratory infection (fever and at least one sign/symptomof respiratory disease (e.g. cough, shortness breath)) AND who requireshospitalization AND who has no other etiology that fully explains the clinicalpresentation.
Exclusion
Exclusion Criteria: Participants eligible for this Trial must not meet any of the following criteria:
Maternal lung pre-existing disease
Maternal cardiac problems
Severely ill patients in unstable condition requiring immediate life-saving procedures Participants who meet one or more of the above exclusion criteria must not proceed to beenrolled in the Trial and will be identified on the Screening Log as Screen Failure.
Study Design
Study Description
Connect with a study center
University Hospitals Leuven
Leuven, 3000
BelgiumActive - Recruiting
University of Brescia
Brescia,
ItalySite Not Available
University of Foggia
Foggia,
ItalySite Not Available
University of Milan
Milan,
ItalySite Not Available
University of Parma
Parma,
ItalySite Not Available
Fondazione Policlinico Universitario A. Gemelli
Roma,
ItalyActive - Recruiting
Queen Charlotte's & Chelsea Hospital
London,
United KingdomSite Not Available

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