Hypertension Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- You are willing and able to give your consent to take part in the study
- You are male or female, aged between 30 and 40 years old at the time of joining
- You previously took part in the ALSPAC study
- You are able and willing to follow all the requirements of the study
- You can read and understand English and can understand spoken English
Who may not be able to join:
- You are currently pregnant or breastfeeding at the time of your first study visit
- It has been less than six months since you gave birth
- You are planning to donate blood within two weeks before your first study visit
- You have a significant illness or condition that, in the opinion of the study doctor, could affect your ability to take part
- You have a heart condition present from birth, or a long-term condition that significantly affects your heart or metabolism
- You are found to be unsuitable for an MRI scan based on a screening check — though you may still be able to take part in other parts of the study
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Adam J Lewandowski, Cardiovascular Clinical Research Facility
Phone: 01865 226845
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Cardiac right ventricular mass
Can't join this trial?
Data last synced from ClinicalTrials.gov: 21 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.