Actively Recruiting

Age: 18Years - 80Years
All Genders
ID03224312

Chongqing Primary Aldosteronism Study Observing Cardiovascular and Kidney Outcomes in Hypertensive Patients

Led by Chongqing Medical University · Updated on 2023-09-06

1500

Participants Needed

1

Research Sites

52 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are conducting a series of clinical studies on primary aldosteronism (PA) and essential hypertension to create a large group of patients for long-term follow-up. They aim to study cardiovascular events, kidney outcomes, and other health effects over up to 15 years. The study also involves collecting samples like blood, urine, and adrenal tissue to build databases of genetic, metabolic, and protein information to better understand PA and related organ damage. Participants include people with PA and essential hypertension who are screened and classified following guidelines. There is no intervention or treatment given as part of the study. Instead, the research focuses on observing and analyzing the participants over time, including those diagnosed with PA and those without it. During the study, participants will be followed for 1 to 15 years with assessments of cardiovascular events, kidney function using estimated glomerular filtration rate (eGFR), the occurrence of atrial fibrillation, changes in heart structure, artery thickness, and quality of life. Researchers will collect and analyze biological samples and health data to explore risk factors, diagnostic methods, and biomarkers. The total participation time depends on individual follow-up within the study period ending in 2028.

CONDITIONS

Brief Title

Chongqing Primary Aldosteronism Study

Who Can Participate

Age: 18Years - 80Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Hypertensive patients who have completed aldosterone-renin ratio (ARR) screening and necessary further tests
  • Voluntary agreement to sign informed consent
  • Age between 18 and 80 years
Not Eligible

You will not qualify if you...

  • Patients with severe cardiac, hepatic, or renal dysfunction
  • Patients with suspected or confirmed other types of secondary hypertension such as Cushing's syndrome, pheochromocytoma, or renal artery stenosis

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Long-term Monitoring

Duration - 1 to 15 years

Participants are observed over an extended period to monitor cardiovascular and kidney outcomes, including events such as atrial fibrillation and changes in kidney function.

Regular visits over several years as scheduled by the study team

Trial Site Locations

Total: 1 location

1

Qifu Li

Chongqing, Chongqing Municipality, China, 400016

Actively Recruiting

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Research Team

Q

Qifu Li, phD

S

Shumin Yang, phD

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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Published Research Related To This Trial

Outcomes after adrenalectomy for unilateral primary aldosteronism: an international consensus on outcome measures and analysis of remission rates in an international cohort.

Tracy A Williams, Jacques W M Lenders, Paolo Mulatero...

https://pubmed.ncbi.nlm.nih.gov/28576687

Primary Aldosteronism: Changing Definitions and New Concepts of Physiology and Pathophysiology Both Inside and Outside the Kidney.

Michael Stowasser, Richard D Gordon

https://pubmed.ncbi.nlm.nih.gov/27535640

Optimizing the aldosterone-to-renin ratio cut-off for screening primary aldosteronism based on cardiovascular risk: a collaborative study.

Chunxue He, Ruolin Li, Jun Yang...

https://pubmed.ncbi.nlm.nih.gov/38270079