Actively Recruiting

Phase Not Applicable
Age: 18Years - 40Years
All Genders
NCT03762499

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

Led by University of Oxford · Updated on 2026-04-29

750

Participants Needed

1

Research Sites

1034 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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).

CONDITIONS

Official Title

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

Who Can Participate

Age: 18Years - 40Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • 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.
Not Eligible

You will not qualify if you...

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

AI-Screening

AI-Powered Screening

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Trial Site Locations

Total: 1 location

1

Cardiovascular Clinical Research Facility

Oxford, United Kingdom, OX3 9DU

Actively Recruiting

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Research Team

M

Maryam Alsharqi

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

QUADRUPLE

Allocation

NON_RANDOMIZED

Model

PARALLEL

Primary Purpose

DIAGNOSTIC

Number of Arms

2

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