Monitoring COVID-19 Vaccination Response in Fragile Populations

NCT ID: NCT05222139

Last Updated: 2025-03-25

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

8894 participants

Study Classification

OBSERVATIONAL

Study Start Date

2021-05-24

Study Completion Date

2024-11-30

Brief Summary

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The present study is part of ORCHESTRA project, a three-year international research project aimed at tackling the coronavirus pandemic. ORCHESTRA provides an innovative approach to learn from the pandemic SARS-CoV-2 crisis, derive recommendations to further management of COVID-19 and be prepared for the possible future pandemic waves. The ORCHESTRA project aims to deliver sound scientific evidence for the prevention and treatment of the infections caused by SARS-CoV-2 assessing epidemiological, clinical, microbiological, and genotypic aspects of population, environment and socio-economic features. The project builds upon existing, and new largescale population cohorts in Europe (France, Germany, Spain, Italy, Belgium, Romania, Netherlands, Luxemburg, and Slovakia) and non-European countries (India, Perú, Ecuador, Colombia, Venezuela, Argentina, Brazil and Gabon) including SARS-CoV-2 infected and non-infected individuals of all ages and conditions. The primary aim of ORCHESTRA is the creation of a new pan European cohort applying homogenous protocols for data collection, data sharing, sampling, and follow-up, which can rapidly advance the knowledge on the control and management of the COVID-19. ORCHESTRA will include SARS-CoV-2-negative individuals and thereby enable a prospective follow-up and an analysis of vaccination response. The cohort will involve four different populations: general population, COVID-19 patients, fragile individuals (children, elderly, transplanted, oncological, HIV infected, and those with Parkinson disease), and health-care workers. Each of these "perpetual" cohorts can answer different research questions and vaccine strategies.

Within the ORCHESTRA project, the Work Package 4 (WP4) will focus on the cohort of fragile patients including pregnant women/new-born, children, patients with HIV infection, patients with autoimmune disease, solid organ transplant recipients, patients with oncological and hematological diseases, patients with cystic fibrosis, patients with Parkinson Disease and rheumatological diseases from from 14 countries (5 European and 9 non-European countries), with approximately 20000 subjects.

Detailed Description

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Since the beginning of COVID-19 pandemic, several special settings have been identified regarding the susceptibility to SARS-CoV-2 infection, the associated clinical spectrum and outcome. The participants include pregnant women, pediatric patients, elderly in particular those whole live in long-term care facilities (LTCFs), and immunocompromised hosts including solid organ transplant recipients (SOT), hematopoietic stem cell transplant (HSCT) recipients and patients with cancer. Among pregnant women and children, asymptomatic or mild diseases have been frequently reported, prompting controversial concerns about their role in the infection transmission in community and hospital settings.

On the other hand, a high impact of COVID-19 on morbidity and mortality has been described in elderly and immuno-compromised hosts. Thus, optimization of prevention strategies, screening practices and therapeutic management is strongly advocated in fragile patients. Indeed, these settings have been established as priority groups for vaccines. However, safety and efficacy of vaccination in these populations should be carefully assessed. Thus, preliminary epidemiological data are strongly needed to design further intervention trials and health policies.

Besides, an increasing body of evidence suggests that the gut microbiota plays a role in determining the severity of COVID-19, possibly through the modulation of immune responses. Furthermore, dysbiosis of the gut microbiota could contribute to the persistence of symptoms, even after the resolution of the disease.

For the same reasons, the microbiota could be involved in the onset of adverse reactions induced by vaccination, especially in fragile populations, as recently discussed. Defining the impact of the microbiota on immunity to vaccination and therefore on its effectiveness is currently considered a priority in various clinical settings.

Moreover, early observations show that vaccines do not induce an immune response conferring protection to many fragile patients, resulting in severe Covid-19 cases. It is important to understand what cellular networks and molecular pathways are switched on/off by the administration of vaccines, and to identify the biological patterns that characterize responders and non-responders. DNA methylation and gene expression analyses may inform on the genomic patterns involved in response to vaccines and in the differences between responders and non-responders. Indeed, DNA sequencing may reveal that the perturbation detected at the regulatory levels may be influenced by alterations in the genome of the divergent subjects.

With this premise, the Investigators deem that a WP dedicated to fragile patients in the ORCHESTRA project is necessary to inform about the peculiarities of the fragile cohort as a whole, and of each subgroup as well, providing clinical and biological information useful to design targeted prevention and therapeutic strategies.

Conditions

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SARS CoV 2 Infection Vaccination; Infection Breakthrough Infection

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Solid organ transplant recipients

Solid organ transplant recipients

COVID-19 vaccination

Intervention Type BIOLOGICAL

Monitoring COVID-19 vaccination

People living with HIV

People living with HIV

COVID-19 vaccination

Intervention Type BIOLOGICAL

Monitoring COVID-19 vaccination

Patients with oncological diseases

Patients with oncological diseases

COVID-19 vaccination

Intervention Type BIOLOGICAL

Monitoring COVID-19 vaccination

Patients with hematological diseases

Patients with hematological diseases

COVID-19 vaccination

Intervention Type BIOLOGICAL

Monitoring COVID-19 vaccination

Patients with cystic fibrosis

Patients with cystic fibrosis

COVID-19 vaccination

Intervention Type BIOLOGICAL

Monitoring COVID-19 vaccination

Patients with Parkinson Disease

Patients with Parkinson Disease

COVID-19 vaccination

Intervention Type BIOLOGICAL

Monitoring COVID-19 vaccination

Patients with rheumatological diseases

Patients with rheumatological diseases

COVID-19 vaccination

Intervention Type BIOLOGICAL

Monitoring COVID-19 vaccination

Pregnant women/ New-borns

Pregnant women/ New-borns

COVID-19 vaccination

Intervention Type BIOLOGICAL

Monitoring COVID-19 vaccination

Children

Children

COVID-19 vaccination

Intervention Type BIOLOGICAL

Monitoring COVID-19 vaccination

Interventions

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COVID-19 vaccination

Monitoring COVID-19 vaccination

Intervention Type BIOLOGICAL

Eligibility Criteria

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Inclusion Criteria

* Any age
* Any comorbidity
* Person (or attorney or deputy who has been authorized to make the decision for patients who lack capacity) consent to participate or appropriate local waiver of consent.

Exclusion Criteria

* Patients did not agree to participate
Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Universita di Verona

OTHER

Sponsor Role collaborator

Hospital Universitario Virgen Macarena

OTHER

Sponsor Role collaborator

Azienda Ospedaliera di Padova

OTHER

Sponsor Role collaborator

Azienda Ospedaliero-Universitaria di Parma

OTHER

Sponsor Role collaborator

Azienda Ulss 2 Marca Trevigiana

OTHER

Sponsor Role collaborator

University College Dublin

OTHER

Sponsor Role collaborator

Luxembourg Institute of Health

OTHER_GOV

Sponsor Role collaborator

Fondazione ICONA

OTHER

Sponsor Role collaborator

University Medical Center Groningen

OTHER

Sponsor Role collaborator

University of Buenos Aires

OTHER

Sponsor Role collaborator

PENTA Foundation

NETWORK

Sponsor Role collaborator

Universiteit Antwerpen

OTHER

Sponsor Role collaborator

Institut National de la Santé Et de la Recherche Médicale, France

OTHER_GOV

Sponsor Role collaborator

Helmholtz Zentrum München

INDUSTRY

Sponsor Role collaborator

CINECA consorzio universitario italiano

UNKNOWN

Sponsor Role collaborator

Charite University, Berlin, Germany

OTHER

Sponsor Role collaborator

Centre de Recherche Médicale de Lambaréné

OTHER

Sponsor Role collaborator

University of Bologna

OTHER

Sponsor Role lead

Responsible Party

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Maddalena Giannella

Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Maddalena Giannella, MD PhD

Role: PRINCIPAL_INVESTIGATOR

University of Bologna

Locations

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Universidad de Buenos Aires (UBA)

Buenos Aires, , Argentina

Site Status

Centre de Recherches Medicales de Lambaréné (CERMEL)

Lambaréné, , Gabon

Site Status

Catholics Bishops Conference of India, Society for Medical Education (CBCI)

Bangalore, , India

Site Status

Translational Health Science and Technology Institute (THSTI)

Faridabad, , India

Site Status

University of Bologna

Bologna, , Italy

Site Status

ICONA Foundation

Milan, , Italy

Site Status

Aziena Ospedaliera Universitaria di Padova - Centro Trapianti di fegato

Padua, , Italy

Site Status

Azienda Ospedaliera Universitaria di Padova - Centro trapianti di polmone

Padua, , Italy

Site Status

Azienda Ospedaliera Universitaria di Padova - UOC Chirurgia dei trapianti di rene

Padua, , Italy

Site Status

Azienda Ospedaliera Universitaria di Padova - UOC Nefrologia Pediatrica

Padua, , Italy

Site Status

Azienda Ospedaliero Universitaria di Padova - Clinica Medica 5

Padua, , Italy

Site Status

Azienda Ospedaliero Universitaria di Padova - Trapianto Multiviscerale

Padua, , Italy

Site Status

Azienda Ospedaliero Universitaria di Padova - UOC Cardiochirurgia

Padua, , Italy

Site Status

Azienda Ospedaliero Universitaria di Padova - UOC Clinica Pediatrica

Padua, , Italy

Site Status

PENTA Foundation

Padua, , Italy

Site Status

Azienda ULSS2 Marca Trevigiana

Treviso, , Italy

Site Status

University of Verona

Verona, , Italy

Site Status

Luxembourg Institute of Health (LIH)

Luxembourg, , Luxembourg

Site Status

University Medical Center Groningen (UMCG)

Groningen, , Netherlands

Site Status

Hosp. Univ. Virgen Macarena / Universidad de Sevilla

Seville, , Spain

Site Status

Countries

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Argentina Gabon India Italy Luxembourg Netherlands Spain

Provided Documents

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Document Type: Study Protocol

View Document

Related Links

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https://pubmed.ncbi.nlm.nih.gov/34450686/

SARS-CoV-2 vaccination in solid-organ transplant recipients: What the clinician needs to know.

https://pubmed.ncbi.nlm.nih.gov/35630462/

Evaluation of the kinetics of antibody response to COVID-19 vaccine in solid organ transplant recipients: the prospective, multicenter ORCHESTRA cohort.

https://pubmed.ncbi.nlm.nih.gov/36636955/

Relationship Between Immune Response to Severe Acute Respiratory Syndrome Coronavirus 2 Vaccines and Development of Breakthrough Infection in Solid Organ Transplant Recipients: The CONTRAST Cohort

https://pubmed.ncbi.nlm.nih.gov/36985328/

Effect of a Fourth Dose of mRNA Vaccine and of Immunosuppression in Preventing SARS-CoV-2 Breakthrough Infections in Heart Transplant Patients.

https://pubmed.ncbi.nlm.nih.gov/37150358/

Using machine learning to predict antibody response to SARS-CoV-2 vaccination in Solid Organ Transplant Recipients. The multicentre ORCHESTRA cohort.

https://pubmed.ncbi.nlm.nih.gov/38005996/

SARS-CoV-2 mRNA Vaccine Response in People Living with HIV According to CD4 Count and CD4/CD8 Ratio.

https://pubmed.ncbi.nlm.nih.gov/38643867/

SARS-CoV-2 mRNA vaccination and short-term changes in viral load and CD4/CD8 T-cell counts in people living with HIV

Other Identifiers

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ORCHESTRA-4

Identifier Type: -

Identifier Source: org_study_id

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