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NCT05052294Active, not recruiting

COVID-19 Antibody Responses in Cystic Fibrosis

COVID-19 Antibody Responses In Cystic Fibrosis: CAR-CF

Source: ClinicalTrials.gov · Last updated 30 Mar 2025

Brief summary (registry, in English)

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 throughout the United Kingdom and other countries. 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.

Status (registry)
Active, not recruiting
Study type
Observational
Enrollment
50 (estimated)
First submitted
21 Sept 2021
Start date
13 Sept 2021
Primary completion date
1 Jun 2025
Lead sponsor
University Hospital, Motol
NCT number
NCT05052294

What you commit to

  • Study type: Observational
  • Planned participants: 50
  • From 13 Sept 2021 to the primary completion date, 1 Jun 2025
  • 2 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • Refusal to give informed consent
  • Contraindication to venepuncture.

Who the study is looking for

  • Consenting people with cystic fibrosis of any age, genotype, transplant status and disease severity

Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (2)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Brno University Hospital
Coordinator of this site? Confirm its status
BrnoCzechiaUnknown status
University Hospital Motol
Coordinator of this site? Confirm its status
PragueCzechiaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.