Nomogram-Based Preoperative Score for Predicting Clinical Outcome in Unilateral Primary Aldosteronism.
Yi Yang, Tracy Ann Williams, Ying Song...
https://pubmed.ncbi.nlm.nih.gov/32898224/Actively Recruiting
Led by Chongqing Medical University · Updated on 2023-09-06
1500
Participants Needed
1
Research Sites
52 weeks
Total Duration
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
Chongqing Primary Aldosteronism Study
Q
Qifu Li, phD
S
Shumin Yang, phD
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here
Chongqing Medical University
Lead Sponsor
You may qualify if you...
You will not qualify if you...
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
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
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
Have more questions? Get in touch with our team for quick support
Yi Yang, Tracy Ann Williams, Ying Song...
https://pubmed.ncbi.nlm.nih.gov/32898224/Silvia Monticone, Jacopo Burrello, Davide Tizzani...
https://pubmed.ncbi.nlm.nih.gov/28385310/Tracy A Williams, Jacques W M Lenders, Paolo Mulatero...
https://pubmed.ncbi.nlm.nih.gov/28576687/Michael Stowasser, Richard D Gordon
https://pubmed.ncbi.nlm.nih.gov/27535640/Chunxue He, Ruolin Li, Jun Yang...
https://pubmed.ncbi.nlm.nih.gov/38270079/Kanran Wang, Jinbo Hu, Jun Yang...
https://pubmed.ncbi.nlm.nih.gov/32449927/Chongqing Medical University
Lead Sponsor