Adrenogenic Autonomic Cortisol Secretion in Chinese Adults
Official title: Chongqing Adrenogenic Autonomic Cortisol Secretion Cohort Study
Run by Chongqing Medical University · NCT05743933 · Data updated 2026-11-12
This study tests whether certain adults with adrenal nodules and cortisol overproduction benefit from personalized treatment strategies for adrenogenic autonomic cortisol secretion.
Quick facts
| Study type | Observational |
|---|---|
| Sex | All |
| Enrollment | 200 (estimated) |
| Sponsor | Chongqing Medical University Academic / other |
| Locations | 1 site (Chongqing, Chongqing Municipality) |
| Status | Recruiting |
| Started | February 17, 2023 |
| Main results expected | February 15, 2033 |
| Study ends | February 15, 2033 |
| Registry record updated | September 24, 2026 |
| Trial ID | NCT05743933 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults with adrenal nodules (max diameter ≥10 mm) and serum cortisol > 50 nmol/L after 1 mg dexamethasone suppression test who consent to participate.
✕Probably not a fit
Patients without autonomic cortisol secretion or those with conditions that mimic MACS may not benefit from the study findings.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This observational cohort prospectively enrolls Chinese adults with adrenal nodules larger than 10 mm and abnormal dexamethasone suppression to characterize etiology, diagnosis, and prognosis of autonomic cortisol secretion. It aims to develop personalized treatment approaches based on function and diagnostic findings, and to follow patients over time to assess outcomes. The study builds on prior data showing MACS is common and linked to higher risks of metabolic and cardiovascular problems, seeking evidence to standardize care. Imaging advances have increased incidentaloma detection, but prospective data on its management remain limited. No interventions are defined in advance for all participants; treatments are determined as part of routine clinical care guided by study findings.
Why it matters
Potential benefit: If successful, the study could inform standardized diagnostic criteria and personalized treatment strategies for MACS, potentially reducing related complications.
How similar studies have gone: Previous retrospective studies suggested associations between MACS and adverse health outcomes, but prospective data are limited and this study seeks to provide new evidence.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * CT examination revealed adrenal nodules (maximum diameter ≥10mm); * Serum cortisol \> 50nmol/L after 1mg dexamethasone inhibition test (1mg-DST). Exclusion Criteria: * Patients with primary aldosteronism (PA), pheochromocytoma, adrenal metastatic carcinoma, congenital adrenal hyperplasia (CAH), ganglionic neuroma/paraganglioma, schwannoma, adrenal hematoma and those with no definite diagnosis were evaluated by clinical and endocrine function. * Patients with serious underlying diseases (such as liver and kidney failure, acute severe infection, etc.) that may affect the function of the hypothalamic-pituitary-adrenal axis (HPA axis); Pregnancy. * Patients with a history of alcoholism, fatigue, trauma, infection, depression, glucocorticoid use, and other drugs affecting the function of the hypothalamic-pituitary-adrenal axis. * Patients who are not willing to participate in and complete this study refuse to sign the written informed consent for this study.
Where it's running
-
Department of Endocrinology, Sichuan-Chongqing Joint Key Laboratory of Metabolic Vascular Diseases, Chongqing Key Laboratory of Translational Medicine in Major Metabolic Diseases, The First Affiliated Hospital of Chongqing Medical University
Chongqing, Chongqing Municipality, China Recruiting
Study contacts
- Principal investigator: Qifu Li, PhD — First Affiliated Hospital of Chongqing Medical University
- Study coordinator: Qifu Li, PhD
- Email: liqifu@yeah.net
- Phone: +86-023-89011552
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.