The Relationship Between ALDH2 and Aortic Dissection
NCT02630212 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 400
Last updated 2019-02-05
Summary
The purpose of this study is to evaluate the impact of ALDH2 Glu504Lys polymorphism on aortic dissection.
Conditions
- Aortic Dissection
Sponsors & Collaborators
-
Qilu Hospital of Shandong University
lead OTHER
Eligibility
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2015-12-31
- Primary Completion
- 2019-12-31
- Completion
- 2019-12-31
Countries
- China
Study Locations
More Related Trials
-
The Proactive Diagnostic Value of Hemostatic Biomarkers in Disseminated Intravascular Coagulation
NCT05995093 ·Status: RECRUITING
-
The Study of Human Atherosclerosis by Polarization-Sensitive Optical Coherence Tomography
NCT00173238 ·Status: UNKNOWN
-
Natural History and Biological Study of Netherton Syndrome
NCT02081313 ·Status: COMPLETED ·Phase: NA
-
Advanced Analysis of the Carotid Phonoangiography and Diseases
NCT02049463 ·Status: UNKNOWN
-
Adiponectin Gene and Coronary Artery Disease
NCT00172991 ·Status: UNKNOWN
-
Mutation Analysis of 17βhydroxysteroid Dehydrogenase 3 Deficiency
NCT00173654 ·Status: UNKNOWN
-
Study of the Causes of the Breakdown of Muscle Fibers in Hospitalized Patients
NCT01022450 ·Status: UNKNOWN
-
Hematological Disorder in Patients With Angiodysplasia
NCT06050798 ·Status: NOT_YET_RECRUITING
-
Studies of Apolipoprotein Genotyping on the Drug Treatment of Hyperlipidemic Patients
NCT00451464 ·Status: COMPLETED
-
Optimizing Diagnosis Of Primary Aldosteronism
NCT02755519 ·Status: COMPLETED
-
Pathological Type,Gene Mutation and Clinical Characteristics of Unilateral Primary Aldosteronism
NCT06597630 ·Status: RECRUITING
-
ACE Gene Polymorphism and ARDS Outcome
NCT00155779 ·Status: COMPLETED
-
Renal Arteries Dysplastic Aneurysms: Anatomopathological and Genetic Study
NCT02528149 ·Status: COMPLETED
-
Biomarkers and Prediction of Tigecycline Induced Coagulation Dysfunction
NCT05698160 ·Status: NOT_YET_RECRUITING
-
Mutation Analysis of 17α-Hydroxylase
NCT00172510 ·Status: UNKNOWN
-
Congenital or Idiopathic Complete Right Bundle Branch Block: Physiological Significance and Molecular Characterization
NCT00173342 ·Status: UNKNOWN
-
The Efficacy and Safety of Anticoagulation in Chinese Patients With Non-ST Segment Elevation Acute Coronary Syndrome
NCT01271101 ·Status: UNKNOWN
-
Significance of Serum Tenascin C in Patients With Acute Aortic Disease
NCT02816892 ·Status: UNKNOWN
-
Normal Reference Values in Han Adults of Extremity Arterial Structure and Hemodynamics by High-frequency Ultrasound
NCT05970926 ·Status: UNKNOWN
-
DNA Typing of HLA-DR/DQ Alleles in Taiwan Chinese With Rheumatic Heart Disease
NCT00264524 ·Status: COMPLETED ·Phase: NA
-
Genomic Study of Congenital Malformation
NCT01250613 ·Status: UNKNOWN
-
Study on Single-nucleotide-polymorphism in Idiopathic Membranous Nephropathy
NCT01799460 ·Status: UNKNOWN
-
The Relationship Between Aortic Pulse Wave and Peripheral Artery Occlusion Disease in Hemodialysis Patients
NCT01945255 ·Status: UNKNOWN
-
The Role of Angiotensinogen Gene Polymorphism in the Pathogenesis of Non-familial Sick Sinus Syndrome
NCT01310920 ·Status: UNKNOWN
-
Genetic Study of Atrial Fibrillation: Focusing on Renin-Angiotensin System and C-Reactive Protein Genes
NCT00173030 ·Status: UNKNOWN