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NCT Number: NCT06108427

REnin-guided TherApy With MinEralocorticoid Receptor Antagonists in Primary Aldosteronism - Feasibility Study

High blood pressure, or hypertension, can be caused by a condition called Primary Aldosteronism (PA), where the body produces too much of a hormone called aldosterone. People with PA have a higher risk of heart problems compared to those with regular high blood pressure. To treat PA, some patients need to take medicine called mineralocorticoid receptor antagonists (MRA) for the rest of their lives. While treatment with MRA is effective, it can have side effects like high levels of potassium in the blood, breast enlargement in men, menstrual problems in women, and reduced sex drive. Finding the right dose of MRA for each patient can be tricky.

Recent observations suggest that when a hormone called renin goes up during MRA treatment, it might be a good sign. This is because renin is higher when the action of aldosterone is well blocked. But it's not certain if this happens because of the patient's unique characteristics or if it can truly be a way to know if the treatment is working.

This study aims to find out if guiding MRA treatment with renin levels leads to more patients having unsuppressed renin levels compared to the standard of care.

This is a multicentric pragmatic clinical trial. Patients with a new diagnosis of PA and low renin levels will be asked if there are willing to participate. Those with recent use of MRA, known MRA intolerance, severe kidney problems, or have high potassium levels will not be able to participate.

Participants will be randomized into two groups: one group will have their MRA treatment adjusted based on renin levels (the "renin-guided" group), and the other group won't have renin levels checked during treatment (the "renin-blinded" group). Both groups will aim to have their blood pressure under control and potassium levels in the normal range.

The main outcome is the proportion in each group with unsuppressed renin levels after 12 months. Other outcomes will be tested, such as changes in renin levels, how well the treatment works, and any safety concerns (like potassium levels, kidney function, side effects, and blood pressure changes). Different groups of patients will also be looked at separately, like men and women, different ages, races, and initial renin levels, to see if the approach works better for some people.

This study will help find a safe and effective way to treat PA with MRA. Choosing the right dose of MRA is important to adequately block aldosterone but also to avoid side effects.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Hôpital du Sacré-Coeur de Montréal

Montreal, Quebec, H4J1C5, Canada

Location status: Recruiting

Location contact

Guylaine Marcotte

CONTACT

Remi Goupil, MD MSc

PRINCIPAL_INVESTIGATOR

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Over 18 years of age
  • Diagnosis of PA, in accordance with clinical guidelines and local practice
  • Suppressed plasma renin prior to treatment initiation (plasma renin concentration >15 mIU/L or >10 ng/L, or plasma renin activity >1 ng/mL/h)
  • Planned long-term treatment with mineralocorticoid receptor antagonist

Exclusion criteria

  • Prior use of mineralocorticoid receptor antagonist or any potassium-sparing diuretics in the past 3 months
  • Known intolerance or contraindication to mineralocorticoid receptor antagonist treatment
  • eGFR < 30 ml/min/1.73m2 (past 3 months)
  • Baseline serum potassium above > 4.8 mmol/L (past 3 months)
  • Deemed medically unsafe to stop medications for the initiation of MRA as monotherapy
  • Pregnancy or breastfeeding
  • Participation in another study that is likely to affect renin or BP levels
  • Inability to provide consent due to cognitive impairment and/or language barrier.

Treatment and study plan

Renin measurements

Other

Use of plasma renin measurements to guide MRA dosing, aiming for plasma renin unsuppression

Primary outcomes

  1. Proportion of participants with unsuppressed renin

    Time frame: 12 months

    Proportion of participants with plasma renin concentration >15 mIU/L or >10 ng/L, or plasma renin activity >1 ng/mL/h

Secondary outcomes

  1. Relative change in renin levels from baseline

    Time frame: 12 months

    Relative change in renin levels from baseline

  2. Office-based systolic and diastolic BP

    Time frame: 12 months

    Office-based systolic and diastolic BP

  3. Central systolic and diastolic BP

    Time frame: 12 months

    Central systolic and diastolic BP

  4. Absolute change in left ventricular mass index from baseline

    Time frame: 12 months

    Absolute change in left ventricular mass index from baseline

  5. Defined daily dose of mineralocorticoid receptor antagonists

    Time frame: 12 months

    Defined daily dose of mineralocorticoid receptor antagonists

  6. Defined daily dose of all antihypertensive medications (including mineralocorticoid receptor antagonists)

    Time frame: 12 months

    Defined daily dose of all antihypertensive medications (including mineralocorticoid receptor antagonists)

  7. Health-related quality of life (SF-36 questionnaire)

    Time frame: 12 months

    Health-related quality of life (SF-36 questionnaire): Score of 0 to 100 with highest better

  8. Health-related quality of life (primary aldosteronism-specific questionnaire)

    Time frame: 12 months

    Health-related quality of life (primary aldosteronism-specific questionnaire): Score of 0 to 112 with highest worse

  9. Albumin/creatinine ratio

    Time frame: 12 months

    Albumin/creatinine ratio

  10. Serum potassium levels

    Time frame: 12 months

    Serum potassium levels

  11. Change in eGFR

    Time frame: 12 months

    Change in eGFR

  12. Proportion of participants with MRA discontinuation, switch or dose-reduction due to side effects or hyperkalemia

    Time frame: 12 months

    Proportion of participants with MRA discontinuation, switch or dose-reduction due to side effects or hyperkalemia

  13. Acute kidney injury (>50% increase in serum creatinine)

    Time frame: 12 months

    >50% increase in serum creatinine

  14. Number of participants with progression towards kidney failure

    Time frame: 12 months

    Number of participants with sustained eGFR loss ≥ 40%, kidney replacement therapy or death from renal failure

  15. Number of participants with symptomatic orthostatic hypotension, dizziness, light headedness, injurious falls, syncope or any unexpected event that the attending physician believes could be attributed to the intervention

    Time frame: 12 months

    Number of participants with symptomatic orthostatic hypotension, dizziness, light headedness, injurious falls, syncope or any unexpected event that the attending physician believes could be attributed to the intervention

  16. Number of participants with cardiovascular adverse events: cardiovascular mortality, myocardial infarction, stroke, heart failure requiring hospitalisation, peripheral artery disease requiring revascularisation (composite and individual categories)

    Time frame: 12 months

    Number of participants with cardiovascular adverse events: cardiovascular mortality, myocardial infarction, stroke, heart failure requiring hospitalisation, peripheral artery disease requiring revascularisation (composite and individual categories)

  17. All-cause hospitalisation

    Time frame: 12 months

    All-cause hospitalisation

  18. All-cause mortality

    Time frame: 12 months

    All-cause mortality

Study contacts

Contact information is provided by the study sponsor or research team.

Remi Goupil, MD MSc

CONTACT

[email protected]

1(514)338-2883

Sponsors and collaborators

Lead sponsor

Centre Integre Universitaire de Sante et Services Sociaux du Nord de l'ile de Montreal

Other

Registry information

Acronym: RETAME-PA

Important dates

Study start
2024
Primary completion
2027
Study completion
2027
First posted
Oct 31, 2023
Registry last updated
Mar 17, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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