Skip to content

Clinical study of chemokine receptor 4 (CXCR4)-mediated precision targeting of 18F for the diagnosis of aldosteronism in primary aldosteronism

Clinical study of chemokine receptor 4 (CXCR4)-mediated precision targeting of 18F for the diagnosis of aldosteronism in primary aldosteronism

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300068930
Enrollment
Unknown
Registered
2023-03-01
Start date
2023-03-01
Completion date
Unknown
Last updated
2023-05-22

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

Conditions

primary hyperaldosteronism

Interventions

Index test:18F-AlF-NOTA-pentiaxther PET/CT

Sponsors

Sichuan Academy of Medical Sciences Sichuan Provincial People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Persistent hypertension or refractory hypertension with blood pressure >160/100 mmHg (blood pressure >140/90 mmHg, combined with three antihypertensive drugs, including diuretics) and hypokalemia. 2. Uncontrolled hypokalemia with or without hypertension. 3. Persistent hypertension or refractory hypertension with blood pressure >160/100mmHg, aldosterone-renin ratio (ARR) >=30 (ng/dl)/(ng/ml/h). 4. A positive captopril test (<=30% reduction in plasma aldosterone levels after captopril administration) is a sufficient but not mandatory condition. 5. Patients whose CT showed unilateral or bilateral adrenal nodules with clear boundaries but normal serum potassium and ARR<30 (ng/dl)/(ng/ml/h) were also included in the study.

Exclusion criteria

Exclusion criteria: 1. Female patients who are pregnant (or pregnant within half a year), breastfeeding or do not want to take contraceptive measures; 2. Abnormal cardiopulmonary function or mental state, unable to tolerate prone lying for 20 minutes; 3. Refused to sign a consent form or unable or unwilling to comply with the approved by the researchers study plan; 4. Other conditions not considered suitable for participation in the study by the researchers.

Design outcomes

Primary

MeasureTime frame
Standardized uptake;Accuracy, specificity, sensitivity;

Secondary

MeasureTime frame
Lesion size;

Countries

China

Contacts

Public ContactZhang Wei

Sichuan Academy of Medical Sciences Sichuan Provincial People's Hospital

zhangwscd@uestc.edu.cn+86 181 1658 0701

Outcome results

None listed

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