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Accuracy of 68Ga-Pentixafor PET/CT for Subtypting Diagnosis in Patients With Primary Aldosteronism Concurrent With Autonomous Cortisol Secretion

Recruiting
Conditions
Primary Aldosteronism Concurrent With Autonomous Cortisol Secretion
Registration Number
NCT06635993
Lead Sponsor
Qifu Li
Brief Summary

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.

Detailed Description

This study is a multicenter, prospective, diagnostic trial involving patients with primary aldosteronism (PA) concurrent with autonomous cortisol secretion (ACS) patients with adrenal nodule (≥1cm) who completed both AVS and 68Ga-Pentixafor PET/CT. We will enroll 97 PA concurrent with ACS patients with adrenal nodule (≥1cm) .The treatment plan was determined according to the AVS results. AVS and/or postoperative remission were used as the reference standard for classification diagnosis to evaluate the accuracy of 68Ga-Pentixafor PET-CT in the classification diagnosis of PA concurrent with ACS patients.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
97
Inclusion Criteria
  1. Getting the written informed consent
  2. The clear diagnosis of primary aldosteronism;
  3. Combined with autonomous cortisol secretion, cortisol after 1mg dexamethasone suppression test (DST) ≥50 nmol/l;
  4. Patients who are willing to undergo surgery;
  5. Adrenal CT or MRI scan of the adrenal glands with nodule (≥1cm).
Exclusion Criteria
  1. 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];
  2. Suspicion of familial hyperaldosteronism or Liddle syndrome. [i.e., age <20 years, hypertension and hypokalemia, or with family history];
  3. Suspicion of pheochromocytoma or adrenal carcinoma;
  4. Patients with actively malignant tumor;
  5. Patients who have adrenalectomy history;
  6. Long-term use of glucocorticoids;
  7. Patients who are allergic to contrast media and cannot tolerate AVS;
  8. Pregnant or lactating women; with alcohol or drug abuse and mental disorders;
  9. Congestive heart failure with New York Heart Association (NYHA) Functional Classification III or IV; History of serious cardiovascular or cerebrovascular disease (angina, myocardial infarction or stroke) in the past 3 months; Severe anemia (Hb<60g/L); Serious liver dysfunction or chronic kidney disease aspartate aminotransferase (AST) or alanine transaminase (ALT) ≥3 times the upper limit of normal, or estimated glomerular filtration rate (eGFR) <30 ml/min/1.73 m2); Systemic Inflammatory Response Syndrome (SIRS); Uncontrolled diabetes (FBG≥13.3 mmol/L); Obesity (BMI≥35 kg/m²); Untreated aneurysm; Other comorbidity potentially interfering with treatment;
  10. Consider patients with bilateral cortisol hypersecretion such as PBMAH or PPNAD.

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
the accuracy of 68Ga-Pentixafor PET-CT in the classification diagnosis of PA concurrent with ACS patient6 months

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.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

The First Affilated Hospital of Chongqing Medical University

🇨🇳

Chongqing, Chongqing, China

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