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Chongqing Primary Aldosteronism Study

C

Chongqing Medical University

Status

Enrolling

Conditions

Primary Aldosteronism

Treatments

Other: no intervention

Study type

Observational

Funder types

Other

Identifiers

NCT03224312
CONPASS

Details and patient eligibility

About

We intends to conduct a series of original clinical research about PA, and establish a large cohort of PA and essential hypertension patients with long-term follow-up of cardiovascular events, renal end points etc. We will establish a large sample of blood, urine, adrenal tissue of the subjects, and the genomics,metabonomics, proteomics database, to explore the mechanism of the PA and target organ damage, risk factors, diagnostic methods and biomarkers.

Full description

This study will include the subjects of a series of studies on hypertension conducted by our team, including essential hypertension, PA subjects, and establish a large sample database and specimen bank through follow-up and omics analysis.

Enrollment

1,500 estimated patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. hypertensive patients who completed ARR screening and necessary further tests;
  2. Voluntary to sign the informed consent.

Exclusion criteria

  1. patients with severe cardiac, hepatic or renal dysfunction;
  2. suspicious or confirmed other types of secondary hypertension, including Cushing's syndrome, pheochromocytoma and renal artery stenosis et al.

Trial design

1,500 participants in 2 patient groups

Primary aldosteronism
Description:
screened, confirmed and subtyped according to the guidelines.
Treatment:
Other: no intervention
Essential hypertension
Description:
screened for PA and excluded the diagnosis of PA as well as other secondary hypertesion
Treatment:
Other: no intervention

Trial contacts and locations

1

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Central trial contact

Qifu Li, phD; Shumin Yang, phD

Data sourced from clinicaltrials.gov

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