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Enrolling by invitation Observational

Prevalence and Predictors of Hypercorticolism in Patients With Difficult to Control Type 2 Diabetes Mellitus

NCT07873320 · tracked via the Priya Life Science Egypt tracker
Phase
Observational
Started
2026-08-30
Last updated
2026-10-14

Condition(s) studied

Detect the Prevalence

Investigational drug(s) / intervention(s)

Over night dexamethasone suppression test

Over night dexamethasone suppression test: Overnight dexamethasone suppression test

Study summary

Type 2 diabetes mellitus (T2DM) is a major global health burden, affecting approximately 589 million adults worldwide in 2024, with the number projected to reach 853 million by 2050 .Despite advances in glucose-lowering therapy, a substantial proportion of patients remain inadequately controlled despite multiple medications .

Hypercortisolism is a potentially reversible contributor to poor glycemic control. Excess cortisol promotes hepatic gluconeogenesis, impairs peripheral insulin sensitivity, and adversely affects β-cell function, thereby contributing to insulin resistance and hyperglycemia .Clinical manifestations of Cushing syndrome may overlap with common features of T2DM and obesity, making mild or clinically unapparent hypercortisolism difficult to recognize .

Recent evidence has highlighted the relevance of hypercortisolism in patients with difficult-to-control T2DM. In the multicenter CATALYST study, 23.8% of 1,057 participants with inadequately controlled T2DM had an abnormal 1-mg dexamethasone suppression test (DST), defined as post-DST cortisol \>1.8 µg/dL (50 nmol/L) . However, data regarding the prevalence and clinical characteristics of hypercortisolism among Egyptian patients with difficult-to-control T2DM are lacking.

The Endocrine Society recommends biochemical testing for suspected Cushing syndrome using validated first-line tests, including the 1-mg overnight DST, late-night salivary cortisol, or urinary free cortisol .Therefore, determining the prevalence and characteristics of hypercortisolism in difficult-to-control T2DM may help identify a potentially treatable contributor to persistent hyperglycemia and provide locally relevant evidence for clinical practice.

Eligibility

Sex
ALL
Min age
18 Years
Max age
70 Years
Healthy volunteers
No
Inclusion Criteria: 1. \- Age: Adults ≥18 years and ≤70 years. 2. \- Diagnosis: Confirmed Type 2 Diabetes Mellitus ≥2 years duration according to ADA criteria. 3- Definition of Difficult-to-Control T2DM: HbA1c ≥8.5% on two separate measurements ≥3 months apart, despite adherence to ≥3 antidiabetic medications including basal insulin ≥0.5 IU/kg/day for a minimum of 6 months. 4- Treatment adherence: Confirmed medication adherence and proper insulin injection technique by clinical assessment + pharmacy refill records 5- Willingness: Signed informed consent to participate in the study and undergo 1mg DST + confirmatory tests Exclusion Criteria: 1. Type 1 DM or any other specific types of diabetes. 2. Pregnancy or lactation- due to physiological hypercortisolism. 3. Current or recent use \<3 months of systemic glucocorticoids, estrogens, oral contraceptives, or drugs affecting cortisol metabolism like ketoconazole, rifampin, phenytoin. Topical/inhaled steroids \<500 mcg/day beclomethasone equivalent are allowed. 4. Known diagnosis of Cushing's syndrome, adrenal tumor, or pituitary disease previously diagnosed. 5. Severe hepatic failure,Child-Pugh C, or severe renal failure, eGFR \<30 ml/min/1.73m² - affect cortisol metabolism. 6. Acute illness, infection, or hospitalization \<1 month- cause stress hypercortisolism. 7. Alcohol abuse\* \>3 units/day for males, \>2 units/day for females. 8. Inability to understand study procedures or give consent. 9. Depression

Primary outcome measure(s)

  • Prevalence of hypercortisolism in patients with difficult-to-control type 2 diabetes mellitus — Baseline
    Percentage of participants with difficult-to-control type 2 diabetes mellitus who meet the predefined diagnostic criteria for hypercortisolism, based on the results of the 1-mg overnight dexamethasone suppression test (ONDST). Unit of Measure:Percentage (%)

Trial sites (1)

FacilityCityRegionStatus
Assiut university hospital Asyut Asyut Governorate
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07873320 on ClinicalTrials.gov ↗ ← All trials in Egypt