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NCT Number: NCT07168122

Establishment and Clinical Application of Reference Intervals of Salivary Cortisol

The goal of this observational study is to establish the normal reference intervals of salivary cortisol and optimal cut-offs for Cushing's sydrome and adrenal insufficiency.

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Key information

Age range

18 year–80 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Shanghai Sixth People's Hospital

Shanghai, Shanghai Municipality, 200233, China

Location status: Recruiting

Location contact

Yufei Zhou, B.S.

CONTACT

[email protected]

16621727469

About this study

Saliva testing is a non-invasive alternative to blood tests for measuring cortisol, a key hormone for assessing endocrine status and diagnosing conditions like Cushing's syndrome. It accurately reflects physiologically active free cortisol. However, its clinical use is hampered by extremely low cortisol concentrations and the lack of reliable detection methods. We have developed two advanced technologies: an immunomagnetic-bead-based LC-MS assay with simplified preparation, and a fluorescence immunoassay system for point-of-care testing. To promote their clinical adoption, this study will establish normal reference intervals of salivary cortisol for both methods in a healthy population and optimal cut-offs in cases of Cushing's sydrome and adrenal insufficiency.

Who can participate

Healthy volunteers accepted: Yes

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

Healthy Volunteers:

Inclusion criteria

  • Age ≥ 18 and ≤ 60 years old;
  • Body mass index (BMI) ≥ 18.5 and ≤ 24.9 kg*m^-2;
  • No previous history of chronic diseases such as hyperglycemia, hypertension, dyslipidemia, coronary heart disease and stroke;
  • Normal glucose regulation, defined as: fasting blood-glucose < 5.6 mmol/L, 2-hour blood-glucose after glucose load < 7.8 mmol/L, and glycated hemoglobin (HbA1c) < 5.7%.

Exclusion criteria

  • Liver or kidney dysfunction, alanine aminotransferase (ALT) or aspartate aminotransferase (AST) or direct bilirubin higher than 1.5 times the upper limit of normal, or serum creatinine >115 μmol/L;
  • Pregnancy or lactation women, or people with cancer or mental illness;
  • Factors affecting cortisol levels, including hypothalamus-pituitary-adrenal axis disease, autoimmune disease (systemic lupus erythematosus, rheumatoid arthritis, etc.), diagnosed mental disease, Alzheimer's disease, alcoholism (alcohol > 60 g/d for male, >40 g/d for women) and corticosteroid therapy in the past 3 months (females with contraceptives or estrogen);
  • Factors affecting saliva collection, such as serious oral problems (oral ulcers, gingival bleeding);
  • Night shift workers, who are awake from 11:00 PM to 7:00 AM;
  • Acute infection (body temperature ≥ 37.3 ℃ or C-reactive protein > 50 mg/L).

Cases:

Inclusion criteria

  • Aged 18 to 80 years old;
  • Patients with suspected Cushing's syndrome or adrenal insufficiency.

Exclusion criteria

  • Corticosteroid therapy within the last 6 weeks;
  • Acute infection;
  • Severe oral conditions;
  • Severe liver and kidney dysfunction;
  • Alcoholism, depression, or other psychiatric disorders.

Treatment and study plan

Primary outcomes

  1. Reference intervals of salivary cortisol

    Time frame: 8:00, 16:00 and 23:00 on the day of sample collection

    Salivary cortisol levels were evaluated by immunomagnetic-bead-based LC-MS assay and fluorescence immunoassay system to establish its reference intervals according to the 2.5th and 97.5th percentiles.

  2. Optimal cut-off and diagnostic accuracy of salivary cortisol in Cushing's syndrome

    Time frame: 23:00 on the day of sample collection

    The diagnostic cut-off for each analysis method was defined as either the calculated upper reference interval (97.5th percentile) or the optimal value determined by the Youden index. The sensitivity, specificity and area under curve for Cushing's syndrome was calculated using samples from all available healthy controls and cases.

  3. Optimal cut-off and diagnostic accuracy of salivary cortisol in adrenal insufficiency

    Time frame: 8:00 on the day of sample collection

    The diagnostic cut-off for each analysis method was defined as either the calculated lower reference intervals (2.5th percentile) or the optimal value determined by the Youden index. The sensitivity, specificity and area under curve for adrenal insufficiency was calculated using samples from all available healthy controls and cases.

  4. Comparison of diagnostic accuracy of salivary cortisol in Cushing's syndrome and adrenal insufficiency

    Time frame: 8:00 or 23:00 on the day of sample collection

    The diagnostic accuracies of the fluorescence immunoassay system and the immunomagnetic-bead-based LC-MS assay were compared by analyzing their areas under the receiver operating characteristic (ROC) curves using DeLong's test for paired statistics.

Secondary outcomes

  1. Agreement in assessment of salivary cortisol

    Time frame: 8:00, 16:00 and 23:00 on the day of sample collection

    To assess the agreement in assessment of salivary cortisol between immunomagnetic-bead-based LC-MS assay and fluorescence immunoassay system

  2. Between-groups differences in salivary cortisol of healthy volunteers with different age ranges

    Time frame: 8:00, 16:00 and 23:00 on the day of sample collection

    Comparsion of salivary cortisol levels in subgroups of age

  3. Between-groups differences in salivary cortisol of healthy volunteers with different sex

    Time frame: 8:00, 16:00 and 23:00 on the day of sample collection

    Comparsion of salivary cortisol levels in subgroups of sex

  4. Between-groups differences in salivary cortisol of healthy volunteers with different body mass index ranges

    Time frame: 8:00, 16:00 and 23:00 on the day of sample collection

    Comparsion of salivary cortisol levels in subgroups of body mass index

Study contacts

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

Jian Zhou, Doctor

CONTACT

[email protected]

+86-021-64369181

Sponsors and collaborators

Lead sponsor

Shanghai 6th People's Hospital

Other

Registry information

Official study title

Study for Reference Intervals and Optimal Cut-offs for Salivary Cortisol

Important dates

Study start
2025
Primary completion
2027
Study completion
2027
First posted
Sep 11, 2025
Registry last updated
Sep 11, 2025

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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