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NCT05614336
COVID-19 Antibody Responses in Cystic Fibrosis
Conditions: COVID-19, Cystic Fibrosis
Sex: All
Phase: NA
Enrollment: 300
Sponsor: Hospices Civils de Lyon
Location: France
Summary
Coronavirus disease 2019 (COVID-19) which is caused by the virus SARS-CoV-2 has resulted in an ongoing global pandemic.
It is unclear whether the relatively low number of reported cases of COVID-19 in people with CF (pwCF) is due to enhanced infection prevention practices or whether pwCF have protective genetic/immune factors.
This study aims to prospectively assess the proportion of pwCF, including both adults and children with CF who have evidence of SARS-CoV-2 antibodies over a two-year period.
This study will also examine whether pwCF who have antibodies for SARS-CoV-2 have a different clinical presentation and what impact this has on their CF disease.
The proposed study will recruit pwCF from paediatric and adult CF centres in Europe.
Serological testing to detect antibodies will be performed on blood samples taken at month 0, 6, 12, 18 and 24 with additional time-points if bloodwork is available via normal clinical care.
Clinical data on, lung function, CF-related medical history, pulmonary exacerbations, antibiotic use, and microbiology and vaccination receipt, will be collected during routine clinical assessments.
Associations will be examined between socio-demographic and clinical variables and serologic testing.
The effects of SARS-CoV-2 infection on clinical outcomes and analyse end-points will be examined to explore any age-related or gender-based differences, as well as subgroup analysis of outcomes in lung-transplant recipients and pwCF receiving CFTR modulator therapies.
As pwCF receive COVID-19 vaccination a comparison of the development and progression of anti-SARS-CoV-2 antibodies in pwCF following natural infection and vaccination SARS-CoV-2 over time will be performed
Eligibility Criteria
Inclusion Criteria:Person with cystic fibrosis of any age, genotype, transplant status and disease severity.Express consent obtained after informing the patient and/or his legal representatives or parents In France, written and informed consent will be requested.For France, affiliation to a social security scheme or similarExclusion Criteria:Refusal to give informed consentContraindication to venepunctureFor FrancePerson under guardianship / curatorshipPerson under legal protection
Source: ClinicalTrials.gov (NCT05614336). StuddyBuddy aggregates publicly available trial information.