Updated Diagnostic Cortisol Values for Adrenal Insufficiency
Montefiore Medical Center · with Medical College of Wisconsin · NCT05149638
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 18+ · All sexes
- Healthy volunteers
- Accepted
- Study type
- Interventional · Not applicable
- Target enrollment
- 90
- US sites recruiting
- 1
- Study start
- February 3, 2022
- Record last updated
- February 19, 2026
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
The purpose of this study is to determine the cortisol levels that most accurately diagnose a patient with adrenal insufficiency, a condition in which cortisol levels are too low for daily living.
Being studied: Cosyntropin stimulation test
Conditions: Adrenal Insufficiency
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Inclusion Criteria for healthy volunteers
- Male and female outpatients 18 years or older without prior diagnosis of primary or central adrenal insufficiency
Inclusion Criteria for patients with known adrenal insufficiency:
- Males and females 18 years or older with established diagnosis of primary or central adrenal insufficiency as previously documented in the electronic medical record by a failed CST (peak cortisol level \< 18 μg/dL) or morning serum cortisol \< 3 mcg/dL with an appropriate clinical circumstance (e.g., Sheehan's syndrome, pituitary surgery and/or irradiation, bilateral adrenalectomy, etc.) that strongly supports a true diagnosis of primary or central adrenal insufficiency, and current use of physiologic, replacement dose glucocorticoids. Inpatients with non-critical illness and outpatients are eligible
Inclusion Criteria for patients with suspected adrenal insufficiency:
- Males and females 18 years or older with suspected diagnosis of primary or central adrenal insufficiency by any cause based on clinical evaluation by a study team member. Inpatients with non-critical illness and outpatients are eligible
Exclusion Criteria for all groups
- Moderate to severe liver impairment or abnormal albumin or cortisol binding globulin concentrations
- Renal impairment with estimated Glomerular Filtration Rate (eGFR) \< 60 mL/min/1.73m2 and/or diagnosis of nephrotic syndrome
- Pregnancy or nursing mothers
- Use of estrogen preparations
- Uncontrolled major depressive disorder or psychiatric diseases, severe malnutrition, eating disorders, chronic fatigue syndrome (disorders that alter hypothalamic-pituitary-adrenal (HPA) axis function)
- Use of any medications that induce hepatic cytochrome P-450 enzymes, e.g., barbiturates, phenytoin, rifampin, aminoglutethimide and mitotane
- Active medical treatment of Cushing's syndrome (status-post surgical treatment is acceptable)
- Uncontrolled hypo- or hyperthyroidism
- Use of biotin within the past 72 hours
- Regular alcohol and/or cannabis use
- History of bilateral adrenalectomy
- Treatment for validated primary adrenal insufficiency for greater than 6 months
- Be assessed by the investigators as unsuitable for participation in this study for any reason
Additional Exclusion Criteria for healthy volunteers only:
- Regular use of any oral glucocorticoid (e.g. hydrocortisone, prednisone, dexamethasone) within 6 weeks of the screening visit
- Use of oral or nasal steroid (glucocorticoid) inhalers in the past 2 weeks
- Regular use of any steroid creams, gels, ointments, or lotions
- Use of steroid (glucocorticoid) injections in the past 6 months (healthy volunteers)
- Regular use of opioids
- Regular use of suboxone
- Regular use of megestrol acetate
Recruiting US locations
Montefiore Medical Center
The Bronx, NY 10467
Site contact: Smita Abraham, MD · smabraham@montefiore.org
Study contacts (from the official record)
- Smita B Abraham, MD · 718-839-7322 · smabraham@montefiore.org
- Noah Bloomgarden, MD · nbloomga@montefiore.org
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