San Gerardo Hospital
Monza, Lombardy, 20900, Italy
NCT Number: NCT05074706
The main objective of this study is to investigate the humoral immune response to COVID-19 vaccines in haematological patients, by testing SARS-CoV-2 seroconversion
Looking for future studies?
Notify Me18 year and older
All sexes
Observational
Monza, Lombardy, 20900, Italy
This single-center prospective study will enroll approximately 700 hematologic patients who access to Haematological Division (San Gerardo Hospital, Monza, Italy) in order to perform their routine blood tests to monitor their hematological conditions. Evaluation of Sars-Cov-2 IgG specific antibodies will be performed on left-over biological material (serum or plasma) collected during routine blood tests run between 30 and 60 days after the administration of the second vaccine dose.
Furthermore, in each patient who has failed seroconversion (absence of specific antibodies for circulation), his cellular immune response will be assessed using an additional blood sample collected during routine blood tests.
These samples will be collected within 9 months of the completion of the vaccination series and will be used to evaluate the plasma INF-γ release using QuantiFERON SARS-CoV-2 test.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Samples will be collected between 30 and 60 days after second vaccine dose.
Other names: Blood serum SARS-CoV-2 IgG
Samples will be collected within 9 months after completion of the vaccination series
Other names: Plasma INF-γ
Time frame: Between 30 and 60 days after the administration of the second vaccine dose
Seroconversion is defined as a post-vaccination SARS-CoV-2 IgG antibody titer >33.8 Binding Anticorpal Unit (BAU)/ml.
Time frame: Between 30 and 60 days after the administration of the second vaccine dose
Time adjusted rate of seroconversion after vaccination in hematological patient and healthy population.
Time frame: Between 30 and 60 days after the administration of the second vaccine dose
Rate of seroconversion per type of haematological condition
Time frame: Between 30 and 60 days after the administration of the second vaccine dose
Rate of seroconversion per specific treatment.
Time frame: Within 9 months after the administration of the second vaccine dose
Rate of patients with a positive RT-PCR-SARS-CoV-2 test in the 9 months after the administration of the second vaccine dose
Time frame: Within 9 months after the administration of the second vaccine dose
Rate of patients with a positive QuantiFERON-SARS-CoV-2 test after the demonstration of seroconversion failure until the end of the study
University of Milano Bicocca
Other
Evaluation of the Immune Response to Sars-Covid-19 (Cov-2) Vaccines in Haematological Patients: Prospective Single Center Study
Acronym: Hema-C19-Vax
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT02343965
Anxiety Disorders, Hematologic Diseases
Nantes, France
View Trial DetailsNCT06187831
Bleeding, Blood Platelet Disorders
Lund, Lunds Universitet, Sweden
View Trial DetailsNCT03578367
Bone Marrow Diseases, CML
Augusta, Georgia, United States
View Trial DetailsNCT03030248
Bacterial Infections, Bacterial Infections and Mycoses
Milwaukee, Wisconsin, United States
View Trial Details