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UnknownNCT06183554

CXCR4 Targeted PET Imaging in the Diagnosis and Identification of Primary Aldosteronism

Status
Unknown
Phase
Study type
Observational
Enrollment
60 (estimated)
Sponsor
Xiao Chen · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

This study aimed to prospectively evaluate the utility of C-X-C chemokine receptor type 4 (CXCR4) positron emission tomography (PET) imaging in patients with clinical suspected primary aldosteronism (PA), with postoperative pathological or follow-up results as reference standards.

Detailed description

1. Record the course of disease, the laboratory examination (e.g., potassium, aldosterone, aldosterone-to-renin ratio, intravenous salt-loading test or captopril test) and the results of adrenal vein sampling in patients with clinically suspected PA. 2. PET image analysis: Record and evaluate the following indicators: the maximum standardized uptake value (SUVmax) of lesions, the mean standardized uptake value (SUVmean) of normal liver, the SUVmean of adjacent normal adrenal tissue, the ratio of the lesional SUVmax to the normal liver SUVmean (LLR), and the ratio of the lesional SUVmax to the adjacent adrenal tissue SUVmean (LAR). 3. Pathological analysis: Hematoxylin and eosin staining and immunohistochemical analyses will be performed. Immunohistochemical analysis will be used to investigate the expression of aldosterone synthase (CYP11B2) and CXCR4.

Conditions

Interventions

TypeNameDescription
DIAGNOSTIC_TESTCXCR4Patients with clinical suspected primary aldosteronism will receive a CXCR4 PET imaging.

Timeline

Start date
2023-08-31
Primary completion
2025-08-31
Completion
2025-08-31
First posted
2023-12-27
Last updated
2024-01-03

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT06183554. Inclusion in this directory is not an endorsement.