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Determinants of the Level of Anti-SARS-CoV-2 IgG ANTibodiEs After Vaccination Study in Patients After Organ Transplantation

Determinants of the Level of Anti-SARS-CoV-2 IgG ANTibodiEs After Vaccination in Patients After Organ Transplantation (DANTE-SIRIO 8) Study

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05162456
Acronym
DANTE-SIRIO 8
Enrollment
250
Registered
2021-12-17
Start date
2021-07-01
Completion date
2023-04-30
Last updated
2021-12-17

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

Conditions

SARS-CoV2 Antibodies, SARS-CoV2 Infection

Brief summary

Great expectations to control the pandemic are placed in vaccines against COVID-19. Currently, the four COVID-19 vaccines approved in the European Union. The investigators designed a study assessing the anti-SARS-CoV-2 IgG antibody titer after vaccination cycle with the BNT162b2 vaccine in several time points relating these results to the COVID-19 history and severity of symptoms during the disease and after the first and second vaccine dose.

Detailed description

The study includes patients of Antoni Jurasz University Hospital No.1 in Bydgoszcz after organ transplantation. To meet the inclusion criteria patients will have to be vaccinated with two doses of the BNT162b2 vaccine. The assessment of the anti-SARS-CoV-2 IgG antibody titer at several time points in each participant. Fresh serum samples were used to measure SARS-CoV-2 IgG on the Siemens Atellica system (Siemens Healthineers, Erlangen, Germany). Results of SARS-CoV-2 IgG were given as U/ml, whereby the cut-off for positivity was defined as ≥1.0 U/ml.

Interventions

evaluation of anti-SARS-CoV-2 IgG antibodies in patients after 2-dose vaccination schedule willing to receive a 3rd dose of vaccine

evaluation of anti-SARS-CoV-2 IgG antibodies in patients after 2-dose vaccination schedule unwilling to receive a 3rd dose of vaccine

Sponsors

Collegium Medicum w Bydgoszczy
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Provision of informed consent to study * Age ≥ 18 years * Receiving two doses of the BNT162b2 vaccine * patients post organ transplantation

Exclusion criteria

* patients who did not complete 2-dose vaccination schedule * patients who received any other vaccine than BNT162b2 * patients considered by investigator to be unable to cooperate

Design outcomes

Primary

MeasureTime frameDescription
the anti-SARS-CoV-2 IgG antibody concentration 3 months after vaccination cycle with the BNT162b2 vaccine0-12 monthsevaluation of anti-SARS-CoV-2 IgG antibody concentration 3 months after 2-dose vaccination with BNT162b2 vaccine

Secondary

MeasureTime frameDescription
the anti-SARS-CoV-2 IgG antibody concentration 6, 9 and 12 months after two-dose vaccination cycle0-12 monthsevaluation of anti-SARS-CoV-2 IgG antibody concentration at particular time points in 2-dose vaccination schedule
the anti-SARS-CoV-2 IgG antibody concentration immediately before, 1 and 3 months after the third vaccine dose0-12 monthsevaluation of anti-SARS-CoV-2 IgG antibody concentration at particular time points after 3rd dose of vaccine
local and/or systemic adverse reactions after vaccination0-12 monthsverification of any adverse events occurrence based on survey filled by participants on each visit
confirmed COVID-19 after vaccination0-12 monthsverification of COVID-19 based on survey filled by participants on each visit

Countries

Poland

Contacts

Primary ContactEmilia Wojtal, MD
terenia4@interia.pl+48 52 5854380

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026