SARS-Cov2 Clinical Trial
— COVID-19Official title:
Observational Study for SARS-Cov2 Epidemiological Surveillance on Healthcare Workers and Patients in a Rehabilitation Medicine Facility
Verified date | June 2023 |
Source | IRCCS San Raffaele Roma |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
The recent SARS-CoV2 pandemic has highlighted that the transmission of the virus within health care facilities plays a fundamental role in its propagation and, therefore, in the increase in COVID-19 cases registered among patients and healthcare workers. This study, original for the current lack of data on nosocomial transmission mechanisms compared to what happens in the community, proposes to conduct a study in patients, health workers and people in real-life setting. The study will be monocentric and performed at the San Raffaele Pisana Institute in Rome, that is able to guarantee the necessary number and the right case-mix that will allow to evaluate any possible correlations between infection and pre-existing disease.
Status | Completed |
Enrollment | 500 |
Est. completion date | December 31, 2020 |
Est. primary completion date | December 31, 2020 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Patients/Participants > 18 years - Subjects who agree with the study signing the informed consent Exclusion Criteria: - Age <18 years; - Pregnancy in progress; - Simultaneous participation in another clinical study - Ongoing immunosuppressive therapy or during the last month |
Country | Name | City | State |
---|---|---|---|
Italy | IRCCS San Raffaele Pisana | Rome |
Lead Sponsor | Collaborator |
---|---|
IRCCS San Raffaele Roma |
Italy,
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* Note: There are 12 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Number of participants with positive RT-PCR against SARS-CoV2 | All subjects will have 3 swabs done and analyzed | 15 days | |
Secondary | Number of participants with qualitative IgM/IgG positive results | All subjects will have 1 blood pick-test | 15 days |
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