Cardiovascular Longitudinal ALSPAC Research Investigations Following Hypertensive Pregnancy in Young Adulthood
Recruiting · NCT05683093 · Observational (researchers observe without assigning treatment) · Lead sponsor: University of Oxford
View the official record on ClinicalTrials.gov →Interventions studied
History of being born to hypertensive or normal pregnancy
What this trial is about
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.
Who can take part
Age range
30 Years to 40 Years
Sex
All (male and female)
Healthy volunteers
No - a diagnosis or condition is required
Phase
Not specified
Study type
Observational (researchers observe without assigning treatment)
Inclusion criteria
- 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
- Adequate understanding of verbal and written English
Exclusion criteria
- 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
- Evidence of congenital heart disease or significant chronic disease relevant to cardiovascular or metabolic status
- For exclusion of MRI component only:
- Unsuitable for MRI based on participant screening; the participant may still be included in other parts of the study
Where it is running
1 location listed.
- University of Oxford - Oxford, Oxfordshire, United Kingdom