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CompletedNCT01567111MIAUpdated Mar 11, 2019

11C-Metomidate PET Versus Adrenal Vein Sampling in Primary Aldosteronism

An interventional study of 11C-Metomidate Positron Emission Tomography in Primary Hyperaldosteronism, sponsored by Helsinki University Central Hospital. Completed at 3 sites in Finland. Open to participants aged 20 Years to 65 Years. Per ClinicalTrials.gov, last updated 2019-03-11.

Sponsored by Helsinki University Central Hospital · Not applicable, Interventional, and Diagnostic

Phase
Not applicable
Study type
Interventional
Enrollment
40
Allocation
Not applicable
Ages
20 Years to 65 Years
Sex
All
01

Study summary

Rationale: Primary hyperaldosteronism (PA) is the most frequent and possibly curable form of secondary hypertension. The diagnosis and targeted treatment of PA is essential because of high vascular morbidity associated with PA as compared to essential hypertension with comparable blood pressure levels. PA is usually caused by either a unilateral aldosterone-producing adenoma (APA) or by bilateral adrenal hyperplasia (BAH). Distinction between APA and BAH is critical since the former may be cured by adrenalectomy, and the latter needs life-long medical therapy with mineralocorticoid receptor antagonists (MRA). Studies demonstrate that adrenalectomy benefits also BAH patients with dominant nodule(s) producing the most of aldosterone excess. The distinction between unilateral and bilateral PA can be made by adrenal vein sampling (AVS), as recommended by The Endocrine Society 2008 guideline. Currently, in Finland the diagnosis is based on computed tomography (CT) scanning which does not distinguish between aldosterone-producing and common non-functioning adrenal nodules and has limited accuracy detecting small adrenal masses. Since AVS is invasive, dependent on skilled radiologist and costly, there is a need for an accurate, non-invasive functional imaging such as 11C-metomidate positron emission tomography (MTO-PET).

Objective: To assess diagnostic ability of MTO-PET as compared to AVS in PA. Secondary objectives: To compare if standardized uptake values (SUVs)in MTO-PET imaging are similar in histologically diagnosed nodular hyperplasia versus adenoma. To assess the diagnostic accuracy of adrenal CT as compared to MTO-PET and AVS. To assess the complete and partial remission rates (blood pressure response expressed in Daily Defined Dosages, medical therapy, use of potassium supplements) after allocating subjects to MRA-therapy or adrenalectomy at 1 and 5 years.

02

Conditions studied

  • Primary Hyperaldosteronism

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Keywords

  • Primary aldosteronism
  • Aldosterone producing adenoma
  • Bilateral adrenal hyperplasia
  • Metomidate-Positron emission tomography
03

In context

Hyperaldosteronism

193 studies on the registry are indexed under Hyperaldosteronism; 89 are open to participants now.

This study's planned enrollment of 40 is below the median of 60 across 91 interventional studies indexed under Hyperaldosteronism.

Browse Hyperaldosteronism studies →

Lead sponsor

Helsinki University Central Hospital is the lead sponsor of 299 studies on the registry; 60 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
20 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Biochemically proven PA
  • Good general health enabling possible adrenalectomy
  • BMI less than 35

Exclusion criteria

Exclusion Criteria:

  • Any contraindication for AVS, MTO-PET or CT
  • Subjects not willing to consider adrenal surgery
  • Pregnancy
  • Familial PA
  • Suspicion of other tumor than adenoma or hyperplasia in adrenal CT scan
05

Study design

Phase
Not applicable
Primary purpose
Diagnostic
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
40 participants (estimated)

Study arms

  • Experimental
    Subjects with PA

    All study subjects have biochemically confirmed PA and undergo adrenal CT, AVS and MTO-PET to diagnose lateralization of aldosterone production.

    Procedure: 11C-Metomidate Positron Emission Tomography

Interventions

  • Procedure11C-Metomidate Positron Emission Tomography

    Dose of intravenous 11C-Metomidate injection is 440MBq and emission scanning of upper abdomen. PET/CT imaging will be done using the Discovery PET/CT VCT or 690 scanner (General Electric Medical Systems, Milwaukee, WI, USA)

06

What researchers measure

Primary outcomes

  1. Standard uptake value (SUV) in 11C metomidate Positron emission tomography (MTO-PET)

    Mean and maximun SUV-values detect lateralization / no lateralization in aldosterone production in MTO-PET as compared to AVS.

    Time frame: Up to 12 weeks

Secondary outcomes

  1. Standard uptake value (SUV) in 11C metomidate Positron emission tomography (MTO-PET)

    Mean and maximun SUV-values detect lateralization / no lateralization in aldosterone production in MTO-PET as compared to adrenal CT.

    Time frame: Up to 12 weeks

  2. Standard uptake value (SUV) in 11C metomidate Positron emission tomography (MTO-PET)

    Diffences between mean and maximum SUVs in MTO-PET between APA and BAH.

    Time frame: Up to 12 weeks

  3. Blood pressure response

    Daily Defined Dosages of hypertension medical therapy in subjects subjected to MRA or adrenalectomy.

    Time frame: 1 and 5 years

07

Study locations

3 sites
  • Helsinki University Central Hospital
    Helsinki, Finland
  • Tampere University
    Tampere, Finland
  • University of Turku
    Turku, Finland
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 11, 2019, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT01567111
Lead sponsor
Helsinki University Central Hospital
Collaborators
Turku University Hospital, Tampere University
Responsible party
Niina Matikainen (M.D., Ph.D., Specialist in endocrinology, Helsinki University Central Hospital) — Principal investigator
First posted
Mar 30, 2012
Start date
Feb 2012
Primary completion
Aug 2015
Completion
Mar 2019
Last update
Mar 11, 2019

Study contacts

Niina Matikainen, M.D., Ph.D.
principal investigator · Helsinki University Central Hospital

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Mar 2019. You cannot join it, but the record below documents what was studied.

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