Hypertension Trial, Recruiting NCT05765786 Sponsor: Queen Mary University of London Condition: Hypertension
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Hypertension Trial, Recruiting

NCT05765786
Recruiting Not Applicable

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:

  • People who are suspected of having a condition called primary aldosteronism (PA) but have not yet received a confirmed diagnosis, based on certain hormone and blood test results showing low renin levels, higher-than-normal sodium, or lower-than-normal potassium.
  • People who have already been diagnosed with PA but had a previous hormone test result (aldosterone below 277 pmol/L) that would normally be too low to move forward with further testing.
  • People whose aldosterone test results have varied across different tests taken at different times, suggesting the hormone levels may fluctuate.
  • People who are willing to give their consent and take part in the study.

Who may not be able to join:

  • People who are unable to stop taking a type of blood pressure medication called beta-blockers for a 2-week period before the study.
  • People who are currently receiving end-of-life care.

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.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 28 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Principal Investigator: William Drake, Prof, Queen Mary University of London

Phone: +442078827275

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

Status
Recruiting
Phase
Not Applicable
Sponsor
Queen Mary University of London
Registry
ClinicalTrials.gov
Start date
24 February 2023
Est. completion
24 July 2027

Where this trial is recruiting

🇬🇧 United Kingdom

Primary endpoints

Sensitivity and specificity of 24 hour urine tetrahydroaldosterone excretion.

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov