Sharper blood test could uncover hidden cause of high blood pressure

NCT ID NCT07691801

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Recruiting now This study
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Not open to general applications. Only people the study team invites can take part.
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Paused for now. It may or may not start again.
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Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
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Cancelled before anyone took part.

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First seen Jul 09, 2026 · Last updated Jul 10, 2026 · Updated 1 time

Summary

This study tests whether a more precise lab technique (mass spectrometry) can improve the captopril test used to diagnose primary aldosteronism, a common but treatable cause of high blood pressure. Researchers will measure aldosterone and renin levels in blood samples from healthy volunteers and patients suspected of having the condition. The goal is to establish a new diagnostic cutoff that helps doctors identify this curable form of hypertension more accurately.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
captopril
What this could lead to
If successful, this could lead to a more accurate diagnostic test for primary aldosteronism, helping doctors identify a treatable cause of high blood pressure earlier.
What could go wrong
This is a diagnostic study, not a treatment trial. The new cutoff value may not prove significantly better than current methods, and results may not apply to all populations.

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Study facts

What this study's own registry entry says, in plain language.

Participants

About 800 people

The number the study aims to enrol. It can still change while the study runs.

Started

Apr 2025

Expected to finish

Aug 2026

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Who is studied

1)Healthy Controls to establish physiological suppression limits.2) Patients with suspected PA undergo captopril inhibition test to determine the cut-off point.

Ages

18 to 70 years

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Normal Control Group Inclusion Criteria * Age 18-70 years old * BMI: 18.5-23.9kg/m² * Gender not restricted * Blood pressure: 100-120/60-80mmHg * No history of hypertension * No abnormal nodules found in adrenal CT * Previous blood potassium and electrocardiogram were all within normal ranges * No history of liver or kidney dysfunction, malignant tumors, metabolic diseases or cardiovascular diseases * No medication used Exclusion Criteria * Those with a family history of hypertension or with clinical manifestations of secondary hypertension * Those who have been taking drugs that may affect the RAAS system for a long time (such as contraceptives, steroids, etc.) * Those with cardiac dysfunction or severe arrhythmia and unable to tolerate the test Patients with suspected primary aldosteronism Inclusion Criteria: * Patients with suspected primary aldosteronism in the outpatient setting * Willing to undergo 4-week spironolactone treatment and cooperate with follow-up Exclusion Criteria: * Patients who did not complete the captopril suppression test * Patients with Cushing's syndrome or other endocrine tumors * Patients allergic to spironolactone or with contraindications for its use (such as severe hyperkalemia, eGFR \< 30) * History of liver or kidney dysfunction * Coexisting severe cardiovascular or cerebrovascular diseases * History of malignant tumors * Other types of endocrine hypertension (hyperthyroidism, pheochromocytoma, Cushing's syndrome, etc.) * Renal artery stenosis * Hypokalemia caused by other factors (renal tubular acidosis, Bartter syndrome, Gitelman syndrome, etc.) * Diabetes with HbA1c \> 7.0% or currently using or having used insulin or SGLT2 inhibitor drugs * Taking special medications such as glucocorticoids, immunosuppressants, oral contraceptives, etc

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

How to take part

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  1. The places running it

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  2. The official record

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Contacts and locations

Locations

  • Peking Union Medical Colledge Hospital

    RECRUITING

    Beijing, Beijing Municipality, 456350, China

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