Diagnosing Variable Primary Aldosteronism.

Sponsor
Queen Mary University of London (Other)
Overall Status
Recruiting
CT.gov ID
NCT05765786
Collaborator
(none)
100
1
36
2.8

Study Details

Study Description

Brief Summary

The goal of this observational study is to see if there is a cyclical or exaggerated diurnal variation in aldosterone production in people with Primary Aldosteronism.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    The main questions it aims to answer are:
    • Can we diagnose more people if we used 24 hour urine measurements?

    • In those with high amounts of aldosterone in their urine, is there a variable pattern to their aldosterone production?

    Participants will have a 24 hour urine measurement. They will also have multiple blood tests throughout the day to study the variability in aldosterone secretion.

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    100 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    Do we Miss a Common Subset of Primary Aldosteronism in Which There is Cyclical or Exaggerated Diurnal Variation in Secretion?
    Actual Study Start Date :
    Feb 24, 2023
    Anticipated Primary Completion Date :
    Feb 24, 2026
    Anticipated Study Completion Date :
    Feb 24, 2026

    Outcome Measures

    Primary Outcome Measures

    1. Sensitivity and specificity of 24 hour urine tetrahydroaldosterone excretion. [12 months]

      Can measurement of 24 hour urine tetrahydroaldosterone excretion detect more people with PA than current conventional screening tests?

    Secondary Outcome Measures

    1. Differences in timed day and night urine THA measurements. [12 months]

      We will be measuring the 24 hour urine THA samples in two separate (approximately 12 hours each) collections, one in the day and one at night. We can then study if there are any differences between day time and night time secretion which may help us understand the diurnal variation in aldosterone secretion.

    2. Variation in aldosterone secretion from day series in those with positive 24h urine THA and those with negative 24h urine THA. [12 months]

      This will allow us to study further if the reason why their screening blood test did not meet the threshold for diagnosis.

    3. Complete or partial clinical cure rate of this cohort of patients that qualify for adrenalectomy [12 months]

      Complete clinical cure is daytime home or ambulatory BP < 135/<85mmHg, on no treatment. Partial clinical cure is BP < 135/<85 mmHg on the same or fewer drugs, not including a K+-sparing diuretic.

    4. Complete biochemical cure of PA in this cohort of patients that qualify for adrenalectomy. [12 months]

      This is defined as (whilst off medications that might alter serum potassium or the RAS) by both: normalization of serum potassium and normalization of ARR or elevated ARR and either baseline PAC <190pmol/L, or normal confirmatory test (saline infusion test or captopril challenge test).

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • People with clinically suspected PA but have not met criteria for diagnosis. Suspicion based on low-renin (renin activity <0.5 nmol/h/L or renin mass <5 ng/L), plasma sodium

    140mmol/L or plasma potassium < 4mmol/L.

    • Patients who have been diagnosed with PA and had previous aldosterone samples <277 pmol/L, a level which would normally not qualify for confirmatory testing.

    • Patients with aldosterone results done at different times that indicate variability in production.

    • Willing to consent and participate in the study.

    Exclusion Criteria:
    • Inability to withdraw β-adrenoceptor antagonist therapy for 2 weeks.

    • People on end of life treatment.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Queen Mary University of London London United Kingdom

    Sponsors and Collaborators

    • Queen Mary University of London

    Investigators

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

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Queen Mary University of London
    ClinicalTrials.gov Identifier:
    NCT05765786
    Other Study ID Numbers:
    • 318689
    First Posted:
    Mar 13, 2023
    Last Update Posted:
    Mar 17, 2023
    Last Verified:
    Feb 1, 2023
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Mar 17, 2023