Hypertension Management in Young Adults Personalised by Echocardiography and Clinical Outcome.

ConditionHypertension
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-40
SponsorUniversity of Oxford

About this trial

HyperEcho is a multi-centre longitudinal observational study, to investigate whether baseline transthoracic echocardiography along with routine data collected in the hypertension clinic can guide clinicians to better manage, and improve risk stratification for cardiovascular disease in young adults with hypertension. Participants are characterised as young adult patients aged between 18 to 40 years old and referred to the hypertension clinic to manage their blood pressure. The study visit will be carried out during the planned routine visit of the participants to the hypertension clinics of NHS trusts within England. Routine data will be collected by the assigned nurse for the hypertension clinic as part of the clinical service, and research participation will not affect the clinical progress of the participant. The additional research component to the clinic will be asking the participants for their consent to undergo a research echocardiography scan if it has not been a part of their clinical assessment. Participants will also be asked to consent to the use of their data that has been collected in the hypertension clinic, such as; referral letters, medical history, 24-hour blood pressure monitoring report, ECG, blood samples, body fat composition, and dietary questionnaire. In addition to this, participants will be asked to consent to further review of their data and medical notes during their follow up visits (up to 10 years).

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 18 - 40 years (at the time of their appointment at the hypertension clinic).

Referred for a Hypertension Clinic in England.

Disqualifiers

Unable or unwilling to give valid consent for participation in the study.

Trial design

Design model

Parallel

Treatments tested in this trial

  • Echocardiography scan

    Diagnostic test

    Non-invasive ultrasound imaging of the heart.

Treatment groups

750 Participants
are divided into 2 treatment groups
Group A: Prospective participantsActive comparator 1 intervention
Group B: Retrospective participantsNo intervention 0 interventions

Trial outcomes

Primary outcomes

1

Identification of patient clusters based on echocardiographic and clinical findings

Number of hypertension patient clusters based on echocardiographic and clinical findings

Time frame
Obtained at the first clinical visit

Secondary outcomes

Other outcomes

Sponsors and contacts

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