Actively Recruiting
Prognosis of Primary Aldosteronism: A Prospective Cohort Study
Led by Xinjiang Medical University · Updated on 2026-02-03
5000
Participants Needed
2
Research Sites
304 weeks
Total Duration
On this page
Sponsors
X
Xinjiang Medical University
Lead Sponsor
F
First Affiliated Hospital of Chengdu Medical College
Collaborating Sponsor
AI-Summary
What this Trial Is About
Primary aldosteronism (PA) is the most common cause of secondary hypertension, and patients with PA have a significantly higher risk of developing cardiovascular and renal complications compared with those with essential hypertension. However, PA remains substantially underdiagnosed and undertreated in clinical practice, and relevant research data on the short-term and long-term prognosis of PA patients in the Chinese population are particularly scarce. This is a multicenter, prospective cohort study designed to systematically collect real-world clinical data of PA patients, including baseline clinical characteristics, etiological subtypes, diagnostic and therapeutic strategies, and long-term follow-up outcomes. Through 5 years of standardized follow-up, this study will analyze the differences in treatment efficacy among PA patients with different pathological subtypes (e.g., adrenal adenoma, adrenal hyperplasia), evaluate the short-term therapeutic efficacy and long-term prognosis of PA patients undergoing different treatment modalities including pharmacotherapy, surgery and interventional therapy, and explore the risk factors for adverse clinical outcomes. Ultimately, it will provide high-quality real-world evidence-based data to optimize the clinical diagnosis and management of PA and improve the long-term prognosis of affected patients.
CONDITIONS
Official Title
Prognosis of Primary Aldosteronism: A Prospective Cohort Study
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Aged between 18 and 80 years old
- Biochemically confirmed diagnosis of Primary Aldosteronism according to contemporary guidelines
- Voluntary to sign the informed consent
You will not qualify if you...
- Patients with severe cardiac, hepatic or renal dysfunction
- Diagnosis of secondary hypertension other than Primary Aldosteronism
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 2 locations
1
The First Affiliated Hospital of Chengdu Medical College
Chengdu, Sichuan, China, 610000
Actively Recruiting
2
The First Affiliated Hospital of Xinjiang Medical University
Ürümqi, Xinjiang, China, 830000
Actively Recruiting
Research Team
X
Xiang Xie, PhD
CONTACT
C
Changjiang Deng
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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