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COVID19 Vaccination: Clinical, Laboratory and Cellular Monitoring

COVID19 Vaccination: Clinical, Laboratory and Cellular Monitoring

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04844632
Acronym
SAPIENZAVAX
Enrollment
5000
Registered
2021-04-14
Start date
2021-02-11
Completion date
2022-05-21
Last updated
2021-04-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Care Associated Infection, Health Care Utilization

Keywords

Covid19, Vaccine

Brief summary

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: 1. 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. 2. Assess the quantity (antibody titer) and quality of the anti-Spike immune response induced by vaccination. 3. 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; 4. 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; 5. To evaluate the cell-mediated immune response (CMI) to vaccination against SARS-CoV-2 in a subgroup of vaccinees. Methodology: 1. Administration at baseline of a questionnaire for the collection of clinical data. 2. Perform a blood sample to measure antibody response in vaccinated subjects 3. Administer a questionnaire to evaluate adverse events after vaccination 4. Reassess the antibody response 1 month after complete vaccination and 6 and 12 months after the start of vaccination 5. An antibody assay will be drawn in a subgroup before subjecting the subject to the vaccine. 6. In a subgroup, the blood collected will also be collected in a heparinized tube for the study of cell-mediated immunity. 7. 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.

Interventions

BIOLOGICALVaccine anti-Covid19

Vaccination with AstraZeneca or Pfizer-Biontech anti-Covid19 vaccine

Sponsors

Istituto Superiore di Sanità
CollaboratorOTHER
University of Roma La Sapienza
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 99 Years
Healthy volunteers
Yes

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.

Design outcomes

Primary

MeasureTime frameDescription
Adverse Event Following Immunization - AEFI12 months from immunizationAdverse 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.

Secondary

MeasureTime frameDescription
Antibody response in vaccinated subject1, 3, 6, 12 months from immunizationTo 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.
Anti-Spike immune response1, 3, 6, 12 months from immunizationAssess the quantity (antibody titer) and quality of the anti-Spike immune response induced by vaccination.
Anti- Nucleoprotein (N) induced by natural infection evaluation1, 3, 6, 12 months from immunizationTo 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;
Neutralizing capacity of sera1, 3, 6, 12 months from immunizationto 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
Cell-mediated immune responseTime 0 (before immunization) 3, 10, 21, 30 days; 1, 3, 6 months from immunizationTo evaluate the cell-mediated immune response (CMI) to vaccination against SARS-CoV-2 in a subgroup of vaccinees.

Countries

Italy

Contacts

Primary ContactStefania Basili, MD
stefania.basili@uniroma1.it+393393452523

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 14, 2026