The Relationship Between HHcy and Contrast-induced Nephropathy in Hypertensive Patients After Coronary Artery Diagnosis and Treatment (CONTRAST-CADT)
Homocysteine, Coronary Disease, Angioplasty,Balloon,Coronary
About this trial
This is an interventional treatment trial for Homocysteine focused on measuring Hyperhomocysteinemia, Coronary angiography, Percutaneous coronary intervention, Hypertension, Contrast-induced nephropathy
Eligibility Criteria
Inclusion Criteria:
From November 2015 to April 2017 , all consecutive patients admitted to the participating centers for the patients who undergoing coronary artery diagnosis and treatment(CAG or PCI) will been considered eligible,about 5500 cases.
Exclusion Criteria:
- Who requires long-term peritoneal or hemodialysis.
- Who had been underwent a kidney transplantation.
- Renal failure with a creatinine level >3 mg/dl.
- Who had been received the contrast agent within 2 weeks or had been received metformin, aminoglycoside antibiotics or acetylcysteine within 48 hours.
- Iodine allergy, acute and chronic infections and hyperthyroidism.
- Left ventricular ejection fraction <30%.
- Secondary hypertension.
- Who can not be tolerated ACEI.
- Any other surgical contraindications.
Sites / Locations
- TIAN Jie
Arms of the Study
Arm 1
Arm 2
Arm 3
Active Comparator
Experimental
Experimental
Group A, without hypertension
Group B, hypertension
Group C,hypertension and hyperhomocysteinemia
The patients who will not be taken the drugs of antihypertension and antihomocysteine.
The hypertensive patients with their plasma Hcy levels <10 umol/L will be taken the drugs of antihypertension(Enalapril Maleate Tablets,as the program-based antihypertension)
The hypertensive patients with their plasma Hcy levels ≥10 umol/L will be taken the drugs of antihypertension and antihomocysteine( Enalapril Maleate and Folic Acid Tablets,as the program-based antihypertension)