About this trial
To evaluate the accuracy of 68Ga-Pentixafor PET-CT in the classification diagnosis of primary aldosteronism concurrent with autonomous cortisol secretion patient, using AVS and/or postoperative remission as the reference standard for classification diagnosis.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Getting the written informed consent
The clear diagnosis of primary aldosteronism;
Combined with autonomous cortisol secretion, cortisol after 1mg dexamethasone suppression test (DST) ≥50 nmol/l;
Patients who are willing to undergo surgery;
Disqualifiers
PA patients who meet the by-passing AVS criteria [i.e., younger than 35 years old, spontaneous hypokalemia, adrenal CT indicated unilateral low-density adenoma (≥1cm), plasma aldosterone >300pg/ml];
Suspicion of familial hyperaldosteronism or Liddle syndrome. [i.e., age <20 years, hypertension and hypokalemia, or with family history];
Suspicion of pheochromocytoma or adrenal carcinoma;
Patients with actively malignant tumor;
Trial population
PA concurrent with ACS patients were from The First Affiliated Hospital of Chongqing Medical University, The Affiliated Hospital of Southwest Medical University, The Third Xiangya Hospital of Central South University, The First Affiliated Hospital of Zhengzhou University and Nanjing Drum Tower Hospital.
Trial design
Cohort
Prospective
Treatments tested in this trial
68Ga-Pentixafor PET/CT
Diagnostic testThe patients had a normal diet with no special preparation before 68Ga-Pentixafor PET/CT imaging. The dosage of intravenously injected 68Ga-Pentixafor was calculated based on the patient\'s weight (1.85 MBq \[0.05mCi\]/kg). Local PET/CT scanning of the upper abdomen was performed on a hybrid PET/CT scanner at 10 minutes after the injection of the intravenous tracer, respectively.
Treatment groups
Trial outcomes
Primary outcomes
the accuracy of 68Ga-Pentixafor PET-CT in the classification diagnosis of PA concurrent with ACS patient
To evaluate the accuracy of 68Ga-Pentixafor PET-CT in the classification diagnosis of primary aldosteronism concurrent with autonomous cortisol secretion patient, using AVS and/or postoperative remission as the reference standard for classification diagnosis.
Sponsors and contacts
Click on the lead sponsor to view all of their trials.
Qifu Li
Lead sponsor
Chongqing Medical University
Sponsor institution
The First Affiliated Hospital of Zhengzhou University
Collaborator
The Affiliated Nanjing Drum Tower Hospital of Nanjing University Medical School
Collaborator
The Third Xiangya Hospital of Central South University
Collaborator
The Affiliated Hospital Of Southwest Medical University
Collaborator