Cardiovascular Longitudinal ALSPAC Research Investigations Following Hypertensive Pregnancy in Young Adulthood

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age30-40
SponsorUniversity of Oxford

About this trial

The purpose of this study is to understand more about why young people who were born to a hypertensive pregnancy may have increased risk of high blood pressure and are often at increased risk of heart and blood vessel disease later in life.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Participant is willing and able to give informed consent for participation in the study

Male or female, aged 30 to 40 years at time of enrolment

Participant previously took part in the ALSPAC study

Able (in the investigator's opinion) and willing to comply with all study requirements

Disqualifiers

Pregnant or lactating when they are due to attend for study visit 1

Less than six months postpartum

Planning to donate blood within two weeks prior to study visit 1

Any significant disease or disorder which, in the opinion of the investigator, might influence the participant's ability to participate in the study

Trial population

Of the 200 young adults followed up from the ALSPAC study, 100 will have been born to a hypertensive pregnancy and 100 following an uncomplicated pregnancy. At time of follow-up, they will be 30 to 40 years of age. At the 25-year follow-up in Bristol, there were 610 individuals born to hypertensive pregnancies.

Trial design

Design model

Cohort

Time perspective

Other

Treatments tested in this trial

  • History of being born to hypertensive or normal pregnancy

    Other intervention

    CLARITY is an observational study whereby participants will attend one 4-hr visit the Division of Cardiovascular Medicine, University of Oxford at the John Radcliffe Hospital in Oxford, with the option to split the study visit over two days for convenience. Participants will be invited by the ALSPAC study team to attend a study visit in Oxford where the investigators will use MRI and other imaging modalities to study the brain, heart, liver, kidneys, and vasculature using standardised protocols. A dataset including information from previous follow-up of these cohorts and the detailed pregnancy data available within ALSPAC will be generated by the study team in Bristol and integrated with available data from the Oxford cohorts.

Treatment groups

No treatment groups listed

Trial outcomes

Primary outcomes

1

Cardiac right ventricular mass

Magnetic resonance imaging (MRI) assessment of cardiac right ventricular mass indexed to body surface area (in g and g/m\^2)

Time frame
30-40 years of old

Secondary outcomes

1

Cardiac left ventricular mass

MRI assessment of cardiac left ventricular mass indexed to body surface area (in g and g/m\^2)

Time frame
30-40 years of old
2

Cardiac right ventricular end-diastolic volume

MRI assessment of cardiac right ventricular end-diastolic volume indexed to body surface area (in ml and ml/m\^2)

Time frame
30-40 years of old
3

Cardiac right ventricular stroke volume

MRI assessment of cardiac right ventricular stroke volume indexed to body surface area (in ml and ml/m\^2)

Time frame
30-40 years of old
4

Cardiac left ventricular end-diastolic volume

MRI assessment of cardiac left ventricular end-diastolic volume indexed to body surface area (in ml and ml/m\^2)

Time frame
30-40 years of old

Other outcomes

Sponsors and contacts

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University of Oxford

Lead sponsor

University of Bristol

Collaborator