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New blood test could spot hidden tumors causing high blood pressure

NCT ID NCT01022515

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
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 Results may not be published yet.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.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study looked at whether a new blood marker called EM66 can help doctors tell the difference between high blood pressure caused by rare adrenal tumors (pheochromocytoma or paraganglioma) and regular high blood pressure. Researchers measured EM66 levels in 60 adults with either these tumors or essential hypertension. The goal is to improve diagnosis and avoid unnecessary tests.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

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

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

60 people

The number who actually took part.

Start date

Nov 2008

Finished

Apr 2022

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.

Ages

18 to 90 years

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

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.

Patients with pheochromocytoma/paraganglioma Inclusion criteria : * men \& women, age \> 18 years old * Newly diagnosed patient : suspicion of pheochromocytoma or paraganglioma with elevation of urinary metanephrines and/or normetanephrines along with evidence of tumor which surgical removal is considered (histological findings following surgery will be the gold standard for final diagnosis and inclusion in the study) * During follow-up of a patient with known genetic predisposition to pheochromocytoma/paraganglioma : suspicion of pheochromocytoma or paraganglioma with or without elevation of urinary metanephrines and/or normetanephrines along with evidence of a tumor which surgical removal is considered (histological findings following surgery will be the gold standard for final diagnosis and inclusion in the study) , * Patients with known pheochromocytoma/paraganglioma, whether malignant or not, whether with metanephrine secretion or not, With tumor sites at inclusion in the study * Patients informed and willing to participate in the study * Patients with medical insurance (French social security) Non inclusion criteria * Patients newly diagnosed, recently operated and the histological findings disprove pheochromocytoma or paraganglioma. * patient imprisoned or under legal protection. Patients with essential hypertension Inclusion criteria * men \& women, age \> 18 years old * paired with a patient with pheochromocytoma/paraganglioma for : gender, age (± 5 years) and centre * patient with hypertension. No aetiology was found after initial check up. * Normal 24 hours urinary excretion of metanephrines \& normetanephrines * For women of childbearing potential : effective contraceptive method and negative urinary pregnancy test * Patients informed and willing to participate in the study * Patients with medical insurance (French social security) Non inclusion criteria * Treatment with proton-pump inhibitors in the 8 days before inclusion in the study * Treatment with beta-blockers, antidepressants, Benzodiazepins, dopa, alphamethyl dopa, if this treatment cannot be interrupted during the study (i.e. for approximately 10 days) * patient imprisoned or under legal protection.

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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.

Contacts and locations

Locations

  • CIC 9301

    Lille, 59000, France

  • CIC 9304

    Paris, 75012, France

  • Cardiology Department

    Paris, 75012, France

  • Cic-Crb 0204

    Rouen, 76000, France

  • Endocrinology Department

    Lille, 59000, France

  • Endocrinology Department

    Rouen, 76000, France

  • Endocrinology Department, Gustave-Roussy Institute

    Villejuif, 94000, France

  • Inserm U982/EA 4310; Rouen University (DC2N)

    Mont-Saint-Aignan, 76800, France

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