The Role of Angiotensinogen Gene Polymorphism in the Pathogenesis of Non-familial Sick Sinus Syndrome
NCT01310920 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 400
Last updated 2011-03-09
Summary
Evidence has been documented for the close relationship between the arrhythmia pathogenesis and the gene expression in renin-angiotensin system. However, it remains unclear for involvement of RAS in the pathogenesis of non-familial sick sinus syndrome. The researchers thus investigated the possible relationship between non-familial sick sinus syndrome and the polymorphism and haplotype of the AGT promoter.
Conditions
- Sick Sinus Syndrome
Interventions
- OTHER
-
observation
genotyping
Sponsors & Collaborators
-
China Medical University Hospital
lead OTHER
Principal Investigators
-
Jan-Yow Chen, M.D. · China Medical University Hospital
Eligibility
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2011-02-28
Countries
- Taiwan
Study Locations
More Related Trials
-
Super Chinese Nephrotic Syndrome Registration System (SUCCESS)
NCT03001934 ·Status: RECRUITING
-
Correlation of Preoperative Indices (serum Vit D, Calcium, Phosphorus, FAR, PLR, SII) on Intraoperative Bleeding in CRS
NCT06737198 ·Status: ACTIVE_NOT_RECRUITING
-
Methylation Biosignature in Childhood Chronic Kidney Disease
NCT02022046 ·Status: COMPLETED
-
Pulmonary Artery Involvement in Takayasu's Arteritis
NCT03189602 ·Status: COMPLETED
-
A Study of Drug-Induced Kidney Disease
NCT00729014 ·Status: UNKNOWN
-
ACE Gene Polymorphism and ARDS Outcome
NCT00155779 ·Status: COMPLETED
-
Retrospective Analysis of Renal Prognosis in Patients With Chronic Kidney Disease
NCT03201406 ·Status: UNKNOWN
-
Genetic Polymorphism and Retinopathy of Prematurity: Correlation of Clinical Presentations and Severity
NCT05132257 ·Status: UNKNOWN
-
The Relation Between Serum Level of Amioterminal Propeptide of Type I Procollagen and Diastolic Dysfunction in Hypertensive Patients Without Diabetes Mellitus
NCT00172406 ·Status: COMPLETED
-
The Genetic Study of Primary Angle-Closure Glaucoma
NCT00155857 ·Status: UNKNOWN
-
DNA Typing of HLA-DR/DQ Alleles in Taiwan Chinese With Rheumatic Heart Disease
NCT00264524 ·Status: COMPLETED ·Phase: NA
-
Pathological Type,Gene Mutation and Clinical Characteristics of Unilateral Primary Aldosteronism
NCT06597630 ·Status: RECRUITING
-
Studies of Apolipoprotein Genotyping on the Drug Treatment of Hyperlipidemic Patients
NCT00451464 ·Status: COMPLETED
-
SNP-based Prediction of Recurrence Risk in Kidney Stone Patients
NCT04937192 ·Status: UNKNOWN
-
Adiponectin Gene and Coronary Artery Disease
NCT00172991 ·Status: UNKNOWN
-
Latent TGF-β-binding Proteins Affect the Fibrotic Process in Renal Impairment and Cardiac Dysfunction
NCT04998227 ·Status: RECRUITING
-
Heart Rate Variability in Chronic Kidney Disease Patients
NCT00824577 ·Status: UNKNOWN
-
The Role of SNP of ECM and MMP on the Development of Pathological High Myopia
NCT00172952 ·Status: UNKNOWN
-
Taiwan Cohort - Chronic ThromboEmbolic Pulmonary Hypertension Registry
NCT03667391 ·Status: UNKNOWN
-
The Association of Genetic Polymorphisms With Statin-Induced Myopathy.
NCT00549029 ·Status: UNKNOWN
-
The Efficacy and Safety of Anticoagulation in Chinese Patients With Non-ST Segment Elevation Acute Coronary Syndrome
NCT01271101 ·Status: UNKNOWN
-
Angiotensin Converting Enzyme Gene Polymorphism in Children With Idiopathic Nephrotic Syndrome
NCT00172276 ·Status: COMPLETED
-
Chinese AntiphosPholipid Syndrome cohorT cOllaborative NEtworks
NCT05230017 ·Status: RECRUITING
-
A Research Proposal to Set up an Integrated National Data Bank and Monitoring System and to Establish the Indicators and Risk Factors for Chronic Kidney Disease
NCT01452360 ·Status: UNKNOWN
-
Correlation of Genetic Polymorphism and Livedo Vasculitis
NCT00975871 ·Status: COMPLETED