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Evaluation of the Diagnostic Value of CXCR4-targeted 68Ga-pentixafor PET/CT for Functional Assessment of Adrenal Nodules

Evaluation of the Diagnostic Value of CXCR4-targeted 68Ga-pentixafor PET/CT for Functional Assessment of Adrenal Nodules

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500109522
Enrollment
Unknown
Registered
2025-09-19
Start date
2024-06-25
Completion date
Unknown
Last updated
2025-09-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Primary aldosteronism, Cushing's syndrome, Nonfunctional adenoma

Interventions

Cushing's Syndrome:None
Nonfunctional adenoma:None

Sponsors

Xiangya Hospital Central South University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Inclusion criteria for the Primary Aldosteronism (PA) group: (1) Hypertension (blood pressure >=140/90 mmHg, or use of antihypertensive medication) with or without hypokalemia; (2) Aldosterone-to-renin ratio (ARR) >=30 (pg/mL)/(µIU/mL); or ARR <30 (pg/mL)/(µIU/mL) but confirmatory test positive in patients at high risk of PA; High-risk patients for PA include: unexplained hypokalemia (regardless of blood pressure level), young age, newly diagnosed hypertension, resistant or low-renin hypertension, unexplained atrial fibrillation, adrenal incidentaloma, obstructive sleep apnea, or family history of PA. 2. Inclusion criteria for the Cushing’s Syndrome (CS) group: (1) Typical manifestations of CS, or nonspecific manifestations such as hypertension or diabetes mellitus; (2) Elevated serum or urinary cortisol, and lack of suppression in the overnight 1-mg dexamethasone suppression test or the low-dose (2 mg/day) dexamethasone suppression test. Patients who meet criterion (2) and/or (1) may be considered for inclusion.

Exclusion criteria

Exclusion criteria: Exclusion criteria for primary aldosteronism: (1) Other common secondary hypertension, including hypercortisolism, renal artery stenosis, renal parenchymal hypertension, chromochromatoma, familial primary aldosteronism, and adrenal cortical carcinoma; (2) Patients with potentially positive screening results but who did not undergo confirmatory testing for various reasons; (3) Patients who did not strictly discontinue medications that significantly affect the renin-angiotensin-aldosterone system (RAAS); Exclusion criteria for Cushing's syndrome: (1) Patients with iatrogenic CS; (2) Patients with abnormal screening test results due to psychiatric disorders such as depression, alcoholism, and polycystic ovary syndrome (PCOS) that activate the HPA axis;

Design outcomes

Primary

MeasureTime frame
Postoperative blood pressure changes (systolic and diastolic; assessed at 1, 3, and 12 months);Clinical remission rate (evaluated according to PASO criteria);Postoperative cortisol and ACTH levels of CS: serum cortisol, urinary free cortisol, ACTH (assessed at 1, 3, and 12 months);

Secondary

MeasureTime frame
Postoperative renin, aldosterone, ARR, serum potassium of PA(assessed at 1, 3, and 12 months) ;

Countries

China

Contacts

Public ContactXianghang Luo

Xiangya Hospital, Central South University

xianghangluo@hotmail.com+86 139 7589 9012

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026