- ICH GCP
- Register voor klinische proeven in de VS.
- Klinische proef NCT04844632
COVID19 Vaccination: Clinical, Laboratory and Cellular Monitoring (SAPIENZAVAX)
Primary objective:
1. Monitor adverse events (Adverse Event Following Immunization - AEFI) in vaccinated subjects and analyze the associations with: (a) demographic variables and anthropometric parameters (sex, age, BMI, etc.); (b) socioeconomic-cultural variables; (c) co-morbidities.
Secondary objectives:
- Monitor the antibody response in vaccinated subjects and analyze the associations with: (a) demographic variables and anthropometric parameters (sex, age, BMI, etc.); (b) socioeconomic-cultural variables; (c) co-morbidities.
- Assess the quantity (antibody titer) and quality of the anti-Spike immune response induced by vaccination.
- Evaluate the dynamics of the infection and the protective efficacy of the vaccine against infection / disease by studying the incidence and titre of antibodies against Nucleoprotein (N) induced by natural infection;
- Evaluate the neutralizing capacity of sera vs. a panel of sera selected and analyzed in house and in in vitro microneutralization systems with live virus;
- To evaluate the cell-mediated immune response (CMI) to vaccination against SARS-CoV-2 in a subgroup of vaccinees.
Methodology:
- Administration at baseline of a questionnaire for the collection of clinical data.
- Perform a blood sample to measure antibody response in vaccinated subjects
- Administer a questionnaire to evaluate adverse events after vaccination
- Reassess the antibody response 1 month after complete vaccination and 6 and 12 months after the start of vaccination
- An antibody assay will be drawn in a subgroup before subjecting the subject to the vaccine.
- In a subgroup, the blood collected will also be collected in a heparinized tube for the study of cell-mediated immunity.
- In the event that a subject participating in the study presents during the course of the observation the positivity for the molecular research of SARS-CoV-2 RNA to the oro-nasopharyngeal swab, a new sample will be performed and sent to the Istituto Superiore di Sanità for the search for viral variants.
Studie Overzicht
Toestand
Interventie / Behandeling
Studietype
Inschrijving (Verwacht)
Contacten en locaties
Studiecontact
- Naam: Stefania Basili, MD
- Telefoonnummer: +393393452523
- E-mail: stefania.basili@uniroma1.it
Studie Locaties
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Roma, Italië, 00161
- Werving
- AOU Policlinico Umberto I
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Contact:
- Stefania Basili, MD
- E-mail: stefania.basili@uniroma1.it
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Deelname Criteria
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
Accepteert gezonde vrijwilligers
Geslachten die in aanmerking komen voor studie
Bemonsteringsmethode
Studie Bevolking
Subjects (age> 18) booked for anti-SARS-CoV-2 vaccination at the AOU Policlinico Umberto I.
Subjects will include healthcare personnel, medical students and university staff recruited from Sapienza University of Rome and Umberto I university hospital.
Beschrijving
Inclusion Criteria:
All subjects vaccinated or to be vaccinated at the AOU Policlinico Umberto I and who will agree to join the study.
Exclusion Criteria:
All subjects who refuse to give consent or who have contraindications to vaccination.
Studie plan
Hoe is de studie opgezet?
Ontwerpdetails
Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
|
Adverse Event Following Immunization - AEFI
Tijdsspanne: 12 months from immunization
|
Adverse events (Adverse Event Following Immunization - AEFI) monitoring in vaccinated subjects and analyze associations with: (a) demographic variables and anthropometric parameters (sex, age, BMI, etc.); (b) socioeconomic-cultural variables; (c) co-morbidities.
|
12 months from immunization
|
Secundaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
|
Antibody response in vaccinated subject
Tijdsspanne: 1, 3, 6, 12 months from immunization
|
To monitor the antibody response in vaccinated subjects and analyze the associations with: (a) demographic variables and anthropometric parameters (sex, age, BMI, etc.); (b) socioeconomic-cultural variables; (c) co-morbidities.
|
1, 3, 6, 12 months from immunization
|
|
Anti-Spike immune response
Tijdsspanne: 1, 3, 6, 12 months from immunization
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Assess the quantity (antibody titer) and quality of the anti-Spike immune response induced by vaccination.
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1, 3, 6, 12 months from immunization
|
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Anti- Nucleoprotein (N) induced by natural infection evaluation
Tijdsspanne: 1, 3, 6, 12 months from immunization
|
To assess the dynamics of the infection and the protective efficacy of the vaccine against infection / disease by studying the incidence and titre of antibodies against Nucleoprotein (N) induced by natural infection;
|
1, 3, 6, 12 months from immunization
|
|
Neutralizing capacity of sera
Tijdsspanne: 1, 3, 6, 12 months from immunization
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to evaluate the neutralizing capacity of sera vs. a panel of sera selected and analyzed in house and in in vitro microneutralization systems with live virus
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1, 3, 6, 12 months from immunization
|
|
Cell-mediated immune response
Tijdsspanne: Time 0 (before immunization) 3, 10, 21, 30 days; 1, 3, 6 months from immunization
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To evaluate the cell-mediated immune response (CMI) to vaccination against SARS-CoV-2 in a subgroup of vaccinees.
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Time 0 (before immunization) 3, 10, 21, 30 days; 1, 3, 6 months from immunization
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Medewerkers en onderzoekers
Sponsor
Medewerkers
Studie record data
Bestudeer belangrijke data
Studie start (Werkelijk)
Primaire voltooiing (Verwacht)
Studie voltooiing (Verwacht)
Studieregistratiedata
Eerst ingediend
Eerst ingediend dat voldeed aan de QC-criteria
Eerst geplaatst (Werkelijk)
Updates van studierecords
Laatste update geplaatst (Werkelijk)
Laatste update ingediend die voldeed aan QC-criteria
Laatst geverifieerd
Meer informatie
Termen gerelateerd aan deze studie
Aanvullende relevante MeSH-voorwaarden
Andere studie-ID-nummers
- COVID19 vaccination_Sapienza
Plan Individuele Deelnemersgegevens (IPD)
Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?
Informatie over medicijnen en apparaten, studiedocumenten
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