- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg 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.
Studieoversigt
Status
Intervention / Behandling
Undersøgelsestype
Tilmelding (Forventet)
Kontakter og lokationer
Studiekontakt
- Navn: Stefania Basili, MD
- Telefonnummer: +393393452523
- E-mail: stefania.basili@uniroma1.it
Studiesteder
-
-
-
Roma, Italien, 00161
- Rekruttering
- AOU Policlinico Umberto I
-
Kontakt:
- Stefania Basili, MD
- E-mail: stefania.basili@uniroma1.it
-
-
Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Prøveudtagningsmetode
Studiebefolkning
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.
Beskrivelse
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.
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Adverse Event Following Immunization - AEFI
Tidsramme: 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
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Antibody response in vaccinated subject
Tidsramme: 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
Tidsramme: 1, 3, 6, 12 months from immunization
|
Assess the quantity (antibody titer) and quality of the anti-Spike immune response induced by vaccination.
|
1, 3, 6, 12 months from immunization
|
|
Anti- Nucleoprotein (N) induced by natural infection evaluation
Tidsramme: 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
Tidsramme: 1, 3, 6, 12 months from immunization
|
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
|
1, 3, 6, 12 months from immunization
|
|
Cell-mediated immune response
Tidsramme: Time 0 (before immunization) 3, 10, 21, 30 days; 1, 3, 6 months from immunization
|
To evaluate the cell-mediated immune response (CMI) to vaccination against SARS-CoV-2 in a subgroup of vaccinees.
|
Time 0 (before immunization) 3, 10, 21, 30 days; 1, 3, 6 months from immunization
|
Samarbejdspartnere og efterforskere
Sponsor
Samarbejdspartnere
Datoer for undersøgelser
Studer store datoer
Studiestart (Faktiske)
Primær færdiggørelse (Forventet)
Studieafslutning (Forventet)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Faktiske)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- COVID19 vaccination_Sapienza
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
Studerer et amerikansk FDA-reguleret lægemiddelprodukt
Studerer et amerikansk FDA-reguleret enhedsprodukt
Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .
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