A Study of Females With CF Throughout Pregnancy and Post-partum, and Follow up of Their Offspring
NCT ID: NCT06797206
Last Updated: 2025-10-01
Study Results
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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RECRUITING
60 participants
OBSERVATIONAL
2025-06-12
2028-05-31
Brief Summary
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Additionally the health of offspring in infancy and early life will be studied to understand if further screening investigations or clinical care models should be part of clinical guidelines
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Detailed Description
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The study is called 'MATRIARCH\_CF' and includes 3 related sub-studies:
'Mama' is enrolling participants aged 16 years or older with CF under the care of the Royal Brompton Hospital (RBH) adult CF Unit who are planning a pregnancy or pregnant. The aim is to describe the impact of pregnancy and the first 12-24 months of parenthood in females with CF on their physical and psychological health. Investigations in eight visits include blood tests, lung function, imaging, and interviews.
'Mini' is enrolling biological offspring of people with CF (mothers and fathers) cared for by the RBH Adult CF Service, from birth to age two. The aim is to collect information that will allow for assessment of health outcomes in offspring of parents with CF in the short term. There will be up to four visits over two years with investigations including blood tests, sweat tests, and brain ultrasound.
'Midi' explores the same question as 'Mini' but in the longer term for those aged three-to-six. There will be up to two visits, and they include lung function testing and a lung MRI.
This study is described as 'observational' as investigators will not provide or change any treatment. Participant's health will be monitored with a range of investigations, many of which are optional. Knowledge gained from this study will be used to create guidelines to help families with CF and their medical teams make decisions around pregnancy and their offspring.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Mama
Females with Cystic Fibrosis who are pregnant or planning a pregnancy
No interventions assigned to this group
Mini
Children aged 0-24 months with one biological parent who has a diagnosis of cystic fibrosis
No interventions assigned to this group
Midi
Children aged 3-6 years with one biological parent who has a diagnosis of cystic fibrosis
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* Written informed consent obtained from participant.
* Under the care of Royal Brompton Hospital CF Reproductive and Maternal Health Service
* Age 16 years or above at time of recruitment
* Confirmed diagnosis of CF
* Planning a pregnancy or pregnant at time of recruitment.
* Ability to adhere to the required visits and investigations.
'Mini' sub-study:
* Written informed consent obtained from participant's legal guardian.
* Infants who have one biological parent with a confirmed diagnosis of CF under care of Royal Brompton Hospital Adult CF Service
* Less than 12 months of age at first visit.
* Ability to adhere to the required visits and investigations.
'Midi' sub-study:
* Written informed consent obtained from participant's legal guardian.
* Children who have one biological parent with a confirmed diagnosis of CF who is under the care of Royal Brompton Hospital Adult CF Service.
* Age three to six years at time of visit
* Ability to adhere to the required visits and investigations.
Exclusion Criteria
* Any significant health condition which would cause inability to comply with protocol based on investigator discretion.
* History of lung transplantation
'Mini' sub-study:
* Legal guardians' inability to provide consent to participate in the study.
* Mother of infant has significant comorbidities unrelated to CF which could affect infant outcomes based on investigator discretion.
'Midi' sub-study:
* Legal guardians' inability to provide consent to participate in the study.
* A significant health condition which is known to affect lung function or imaging based on investigator discretion
ALL
No
Sponsors
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Cystic Fibrosis Trust
OTHER
King's College London
OTHER
Imperial College London
OTHER
Royal Brompton & Harefield NHS Foundation Trust
OTHER
Responsible Party
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Principal Investigators
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Imogen Felton
Role: PRINCIPAL_INVESTIGATOR
Royal Brompton Hospital and NHLI Imperial College London
Jane Davies
Role: PRINCIPAL_INVESTIGATOR
Royal Brompton Hospital and NHLI Imperial College London
Locations
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Royal Brompton Hospital
London, , United Kingdom
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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352398
Identifier Type: -
Identifier Source: org_study_id
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