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Congenital Adrenal HyperplasiaMASSALIVENCT07718230

Evaluation of Circadian Hormonal Balance: LC-MS/MS Measurement of Salivary and Serum Steroids in Patients With Congenital Adrenal Hyperplasia

An observational study of Congenital Adrenal Hyperplasia and Adrenal Insufficiency, run by Assistance Publique - Hôpitaux de Paris at 1 site in France.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record
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Trial summary

In congenital adrenal hyperplasia (CAH), lifelong hormone replacement therapy is required to treat adrenal insufficiency and to reduce elevated androgen levels. This is essential to ensure "normal" growth and puberty. Read more about this study

Who is it for?
Ages 6 years and older
How many people
50 participants
Where
1 siteFrance
Study dates
Sep 2026to Sep 2028
Phase
Observational
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 6 years and older
  • All sexes
  • No healthy volunteers
  • Child, Adult, Older adult

Study population: Pediatric patients with congenital adrenal hyperplasia followed in the pediatric endocrinology departments of Hôpital Armand Trousseau (Centre de Référence Maladies Endocriniennes Rares de la Croissance) and Hôpital Bicêtre (Service d'Endocrinologie et diabète de l'Enfant, Centre de Référence DevGen), seen during their routine follow-up visits.

Who may be able to join

  • Patients aged 6 years or older
  • Confirmed diagnosis of congenital adrenal hyperplasia treated with glucocorticoids
  • Signed informed consent provided by legal guardians
  • Affiliation to a national health insurance system

Who cannot join

  • Patients younger than 6 years of age
  • Lesions of the oral mucosa that could interfere with saliva sampling
  • Inability to provide the patient or legal representatives with appropriate study information (e.g., poor understanding of French)
  • Underage parents
  • Lack of affiliation with a social security/health insurance system

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Antonin LAMAZIERE, PU-PH contact

+33 1 40 01 14 90

antonin.lamaziere@aphp.fr

France1 site
  • Service des Explorations Fonctionnelles Endocriniennes, Hôpital Armand Trousseau

    Paris, 75012

    Muriel HOUANG, MD, +33 1 44 73 66 31, muriel.houang@aphp.fr

    Claire BOUVATTIER, MD, +33 1 45 21 22 75, claire.bouvattier@aphp.fr

Other trials in France

About this study

In congenital adrenal hyperplasia (CAH), lifelong hormone replacement therapy is required to treat adrenal insufficiency and to reduce elevated androgen levels. This is essential to ensure "normal" growth and puberty. Replacement therapy includes hydrocortisone and 9α-fludrocortisone acetate (as a mineralocorticoid substitute). Defining appropriate criteria for evaluating therapeutic goals is a key component of patient follow-up.

Currently, monitoring is generally limited to the quantification of serum 17-hydroxyprogesterone (17OHP), testosterone (T) and delta-4 androstenedione (D4), measured in the morning after an overnight fast and before the morning hydrocortisone dose. However, such single-point serum measurements do not take into account the circadian rhythm of these steroids.

The objective of the study is to evaluate correlations between steroid levels (21-deoxycortisol, 17-hydroxyprogesterone, testosterone, delta-4 androstenedione, and cortisol) measured by LC-MS/MS in multiple at-home self-collected saliva samples and those measured in serum during routine monitoring.

Read the detailed description

In this project, in addition to the analysis of circulating steroids routinely performed during semi-annual follow-up, salivary steroid profiling will be performed using mass spectrometry and compared with serum measurements. The study also describe their variations over the nycthemeral cycle in a population of children with CAH. The ability to collect saliva samples at home and throughout the nycthemeral period provides significant advantages. Only five non-invasive salivary self-samples (8 a.m., 12 p.m., 4 p.m., 8 p.m., and 8 a.m.) will be requested as additional collections (1 to 2 times over 12 months). Therefore, this study does not require any additional invasive procedure beyond standard clinical follow-up. Preliminary results have demonstrated the technical feasibility of this approach. The temporal evolution of these profiles may subsequently be modelled using multivariate statistical methods to provide clinicians with innovative tools for improved therapeutic monitoring.

This is a prospective, bicentric, non-interventional observational cohort study conducted in two French pediatric endocrinology centers (Hôpital Armand Trousseau and Hôpital Bicêtre). The study focuses on children with congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency, treated with glucocorticoids according to current clinical practice. CAH is a rare adrenal disorder characterized by adrenal insufficiency and variable degrees of hyperandrogenism. Lifelong hormone replacement with hydrocortisone and 9α-fludrocortisone acetate is required to control androgen excess and ensure normal growth and pubertal development. Therapeutic management must strike a balance between overtreatment (risk of growth retardation, weight gain, osteoporosis, and metabolic and cardiovascular complications) and undertreatment (persistent hyperandrogenism, accelerated growth, menstrual cycle disturbances, and testicular adrenal rest tumors).

Current monitoring relies mainly on single morning serum measurements of steroid profiles, especially 17-hydroxyprogesterone (17OHP), testosterone, and delta-4 androstenedione, generally sampled in the fasting state before the morning hydrocortisone dose. However, several studies have highlighted that these steroids exhibit circadian variation, and a single time-point sample may not adequately reflect overall hormone control or guide treatment optimization.

Advances in liquid chromatography tandem mass spectrometry (LC-MS/MS) now allow highly sensitive and specific profiling of multiple steroids in low-concentration matrices such as saliva. This technique offers improved analytical performance compared with immunoassays, including lower detection limits, better specificity, and the possibility to quantify numerous steroids in a single run. Salivary sampling is non-invasive, feasible at home, and well suited for repeated sampling across the nycthemeral cycle.

In this study, during routine follow-up visits (1-2 times per year), patients will undergo their usual serum sampling performed as part of standard care. In addition, parents and/or patients will collect five saliva samples at home over a nycthemeral cycle (8:00, 12:00, 16:00, 20:00, and the following morning at 8:00). The last salivary sample at 8:00 a.m. will be collected at the hospital on the day of the routine visit, at the same time as the serum sample and before the morning hydrocortisone dose. Thus, for each evaluation, one serum sample and five saliva samples will be available per patient.

Steroid profiling (21-deoxycortisol, 17-hydroxyprogesterone, testosterone, delta-4 androstenedione and cortisol) will be performed on both serum and saliva using LC-MS/MS in the Department of Clinical Metabolomics (METOMICS) at Hôpital Saint-Antoine. The primary analysis will examine the correlation between steroid concentrations measured in saliva and serum at 8:00 a.m. using intraclass correlation coefficients and their 95% confidence intervals. Secondary analyses will characterize nycthemeral salivary steroid profiles and explore their relationship with hydrocortisone and fludrocortisone dosing regimens (dose and schedule). When repeated measurements are available for a given patient, they will be handled as repeated measures in the statistical models.

The planned sample size is approximately 50 CAH patients (about 25 per center), followed for up to 12 months with 1-2 routine visits during the inclusion period. This sample size provides sufficient precision to estimate an intraclass correlation coefficient of at least 0.85 for the primary endpoint. No additional invasive procedures are required beyond standard care; the only supplementary procedures are non-invasive salivary self-samplings performed at home. Biological samples (serum and saliva) will be stored at -20°C for up to 15 months for the purposes of the study, and remaining material may be used for future research on CAH-related steroid profiles in accordance with French regulations and patient consent.

Keywords
Congenital adrenal hyperplasia, 21-hydroxylase deficiency, pediatric endocrinology, salivary steroids, LC-MS/MS, circadian rhythm, nycthemeral profile, hydrocortisone, fludrocortisone, steroid profiling
Medical subject headings
Adrenal Hyperplasia, Congenital, Adrenal Insufficiency, Hyperandrogenism, Congenital adrenal hyperplasia due to 21 hydroxylase deficiency

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT07718230
Study groupRoleWhat they receive
CAH pediatric cohort treated with glucocorticoidsChildren and adolescents with congenital adrenal hyperplasia followed in the participating pediatric endocrinology centers, with 1-2 routine follow-up visits per year, during which paired serum and salivary steroid measurements are obtained.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Correlation between salivary and serum steroid levels at 8:00 a.m.

    Intraclass correlation coefficient between 21-deoxycortisol, 17-hydroxyprogesterone, testosterone, delta-4 androstenedione and cortisol measured by LC-MS/MS in paired salivary and serum samples collected at 8:00 a.m. before the morning hydrocortisone dose.

    Measured: At the routine follow-up visit within 12 months after inclusion

Secondary outcomes (2)
  1. Nycthemeral profile of salivary steroid levels

    Description and quantitative characterization of circadian variation in salivary 21-deoxycortisol, 17-hydroxyprogesterone, testosterone, delta-4 androstenedione and cortisol measured by LC-MS/MS in CAH patients treated with glucocorticoids.

    Measured: Over a 24-hour nycthemeral cycle (8:00, 12:00, 16:00, 20:00, and 8:00 the next morning) within 12 months after inclusion

  2. Correlation between quantitative salivary circadian steroid profiles (ng/mL) obtained by mass spectrometry and hydrocortisone/fludrocortisone dosing (mg/m2 and microg/day respectively)

    Evaluation of the relationship between salivary steroid levels (21-deoxycortisol, 17-hydroxyprogesterone, testosterone, delta-4 androstenedione and cortisol) over the nycthemeral cycle and the type, dose and schedule of hydrocortisone and fludrocortisone treatment.

    Measured: Over a 24-hour circadian cycle during the 12-month observation period

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted21 Jul 2026
  2. Study startSep 2026 (estimated)
  3. Primary completionSep 2027 (estimated)
  4. Study completionSep 2028 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
50 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07718230
Sponsor's protocol ID
APHP240719
Other IDs
IDRCB 2024-A01224-43
Acronym
MASSALIVE
Status last verified
Jul 2026
First submitted
18 May 2026
Last updated
21 Jul 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: Individual participant data (IPD) will not be shared outside the study team. This is a non-interventional observational study in a small pediatric cohort, and no external data-sharing plan has been defined in the protocol or by the sponsor.

Questions about this trial

What is this clinical trial studying?

An observational study of Congenital Adrenal Hyperplasia and Adrenal Insufficiency, run by Assistance Publique - Hôpitaux de Paris at 1 site in France.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: opening soon, as of the sponsor's last update on 21 Jul 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in France. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Muriel HOUANG, MD (+33 1 44 73 66 31, muriel.houang@aphp.fr), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Correlation between salivary and serum steroid levels at 8:00 a.m. (time frame: At the routine follow-up visit within 12 months after inclusion). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 21 Jul 2026.

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