Clinical Trials Logo

Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT05927961
Other study ID # SPP of APA/UAH
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date August 2023
Est. completion date May 25, 2024

Study information

Verified date June 2023
Source Third Military Medical University
Contact Yan Zhencheng, MD
Phone 86-13983656682
Email zhenchengyan@sina.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Primary aldosteronism (PA) is a common cause of secondary hypertension, which is characterized by excessive aldosterone production by the adrenal gland. Excessive aldosterone can significantly increase the risk of cardiovascular disease and stroke. Patients with aldosterone-producing adenoma (APA) or unilateral hyperplasia (UAH) can be cured by unilateral adrenalectomy. The adrenal cortex is the outer part of the adrenal gland and is subdivided into three layers- the zona glomerulosa, the zona fasciculata, and the zona reticularis. And the outermost layer is the zona glomerulosa, and it's full of cells that make the hormone aldosterone. Although it has been investigated that the main cause of APA or UAH is the mutations of different calcium ion channels, including KCNJ5, CACNA1D, CLCN2 et al, it is still unknown whether there are any other changes of other proteins in different layers. Therefore, the investigators designed the study to characterize the proteomics profiles of adrenal adenoma/hyperplasia leading to primary aldosterone and identify biomarkers for early identification of PA by using spatial proteomics. The samples from adrenal adenoma or hyperplasia will be collected and analyzed by spatial proteomics in Hangzhou Jingjie Biotechnology Co., Ltd. The differentially expressed proteins in different layers will be screened out between APA and UAH, APA and its adjacent normal tissues, and UAH and its adjacent normal tissues, respectively. And KEGG analysis will be conducted to determine enriched pathway in these differentially expressed protein, respectively.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 30
Est. completion date May 25, 2024
Est. primary completion date December 30, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria: - According to the 2020 guidelines for primary aldosteronism, patients with positive primary aldosteronism confirmed test; - Patients with predominant unilateral aldosterone secretion at AVS; adrenal CT suggesting unilateral adrenal adenoma (> 0.8cm diameter) and no abnormalities in contralateral adrenal morphology. - Patients who agreed to do the adrenalectomy. Exclusion Criteria: - adrenal CT suggests abnormal bilateral adrenal morphology or unilateral nodules. - glucocorticoids can treat aldosteronism (GRA) and familial aldosteronism. - other secondary hypertension: renal parenchymal hypertension, renal artery stenosis, Cushing syndrome, adrenal myeloid hyperplasia, aortic narrowing, obstructive sleep apnea hypoventilation syndrome. - any other unsuitable condition for surgery. - Patients who refused to perform adrenalectomy.

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
histopathology
There is a clear boundary between adrenal adenoma and surrounding normal tissue. There is no clear boundary between adrenal hyperplasia and surrounding normal tissues.

Locations

Country Name City State
China The Third Affiliated Hospital of the Third Military Medical University Chongqing

Sponsors (1)

Lead Sponsor Collaborator
Third Military Medical University

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Screening for the biomarkers. Histological validation of the CYP11B2 positive area in APA and UAH by immunohistochemical staining (IHC). Some specimens will be characterized more deeply with advanced spatial proteomics technologies to identify the biomarkers. After APA/UAH resection/biopsy, usually within 6 months
Secondary Incorporate biomarkers into the accurate and early diagnosis of PA. Verifying the relationship between biomarkers and clinical presentations, including plasma aldosterone concentrations (PAC), aldosterone to rein ratio (ARR), direct renin concentration (DRC), and serum potassium, etc. Comparing the relationships between biomarkers and risk factors, including osas and family history, etc. Establishing a mathematical model for diagnosing PA through machine learning and studying the pathogenesis of PA through corresponding animal models. 12 months
Secondary Identifying the relationship between biomarkers and the prognosis of PA. The alteration of blood pressure and medication status are investigated through 3 months followed up. Verifying the relationship between the biomarkers and the function of APA and UAH, as well as the prognosis of PA. 12 months
See also
  Status Clinical Trial Phase
Completed NCT05361083 - First-in-human Evaluation of [18F]CETO Early Phase 1
Recruiting NCT04428827 - Outcome of Patients With Primary Aldosteronism
Completed NCT03990701 - Primary Aldosteronism and Surgically Curable Forms in Hypertension Patients Using 11C-Metomidate Early Phase 1
Completed NCT04761354 - Predicting Reduction of Hypertension After Adrenalectomy for Primary Aldosteronism: a Multicenter Analysis
Completed NCT04185857 - MRA and ARB Treatment in Screening of Primary Aldosteronism
Completed NCT04378387 - Ipsilateral and Contralateral Index for the Interpretation of Adrenal Vein Sampling (AVS) in Primary Aldosteronism
Completed NCT03174847 - Prospective Study Assessing Blood Pressure and Other Outcomes Post-treatment in Patients With Primary Aldosteronism
Recruiting NCT06100367 - 11C-Metomidate PET/CT for Endocrine Hypertension and Characterisation of Adrenal Tumours Phase 2/Phase 3
Completed NCT02642445 - Renal Sympathetic Denervation From The Adventitia on Hypertension N/A
Not yet recruiting NCT03449797 - Rapid Cortisol Assay in Adrenal Vein Sampling N/A