Long-term outcomes after treatment for primary aldosteronism
Official title: Prognosis of Primary Aldosteronism: A Prospective Cohort Study
Run by Xinjiang Medical University · NCT07378176 · Data updated 2026-11-12
This project will follow adults with primary aldosteronism for five years to see how different disease subtypes and treatments affect blood pressure, hormone levels, and heart and kidney health.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years to 80 Years |
| Sex | All |
| Enrollment | 5000 (estimated) |
| Sponsor | Xinjiang Medical University Academic / other |
| Locations | 2 sites (Chengdu, Sichuan and 1 other locations) |
| Status | Recruiting |
| Started | January 30, 2026 |
| Main results expected | January 2031 |
| Study ends | December 2031 |
| Registry record updated | February 3, 2026 |
| Trial ID | NCT07378176 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults aged 18–80 with a biochemical diagnosis of primary aldosteronism who can provide informed consent and attend follow-up visits are the intended participants.
✕Probably not a fit
Patients with severe cardiac, hepatic, or renal failure, those with other forms of secondary hypertension, or those unable to attend follow-up visits are unlikely to benefit from participation or be eligible.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This is a multicenter prospective cohort enrolling adults with biochemically confirmed primary aldosteronism at two major hospitals in China. Investigators will collect baseline clinical features, etiologic subtypes, diagnostic approaches, and treatment plans, then perform standardized follow-up visits over five years. The study will compare short-term treatment responses and long-term prognosis across pathological subtypes (for example adrenal adenoma versus hyperplasia) and treatment modalities including medication and surgery. Outcomes include rates of blood pressure and hormonal normalization, trajectories of cardiac, renal and vascular damage, metabolic and cognitive changes, and predictors of cardiovascular events.
Why it matters
Potential benefit: If successful, the findings could help clinicians choose treatments that better normalize blood pressure and reduce heart and kidney complications in patients with primary aldosteronism in China.
How similar studies have gone: International cohort studies have shown subtype-directed management can improve outcomes, but long-term prospective data specifically in Chinese populations are limited, making this multicenter effort relatively novel for China.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. Aged between 18 and 80 years old. 2. Biochemically confirmed diagnosis of Primary Aldosteronism (PA) according to contemporary guidelines (e.g., confirmed positive case detection test and confirmatory test). 3. Voluntary to sign the informed consent. Exclusion Criteria: 1. patients with severe cardiac, hepatic or renal dysfunction; 2. Diagnosis of secondary hypertension other than PA.
Where it's running
-
The First Affiliated Hospital of Chengdu Medical College
Chengdu, Sichuan, China Recruiting -
The First Affiliated Hospital of Xinjiang Medical University
Ürümqi, Xinjiang, China Recruiting
Study contacts
- Study coordinator: Xiang Xie, PhD
- Email: xiangxie999@sina.com
- Phone: +86-991-4366892
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.