EUCTR2015-000239-34-GB进行中(未招募)1 期
T-proBNP selected prevention of cardiac events in a population of diabetic patients without a history of cardiac disease (Pontiac II); a prospective randomized trial - PONTIAC II
试验速览
- 阶段
- 1 期
- 状态
- 进行中(未招募)
- 入组人数
- 2,400
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
入选标准
- •1) Type-2 diabetes mellitus - diagnosed for at least six months prior to inclusion
- •2) = 18 years of age, male or female
- •3) Written informed consent to participate in the study and ability to comply with the study requirements.
- •Are the trial subjects under 18? no
- •Number of subjects for this age range: 0
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 75
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 75
排除标准
- •1) History of hypersensitivity to any of the drugs investigated as well as known or suspected contraindications to the study drugs or previous history of intolerance to high dose of RAAS-antagonists or beta-blocker in the absence of any other blood pressure lowering drugs.
- •2) Patients already receiving a maximum dose of RAAS-antagonists or beta-blocker.
- •3) Creatinine > 2.5mg/dl.
- •4) Symptomatic hypotension and/or systolic blood pressure (SBP) < 100mmHg at visit 1.
- •5) Symptomatic bradycardia and/or heart rate (HR) < 60bpm at visit 1.
- •6) Signs of cardiac disease in the electrocardiogram such as atrial fibrillation; ST-T abnormalities or a bundle branch block/ higher degree AV block.
- •7) Abnormal echocardiography, defined as low ejection fraction < 50%; wall motion
- •abnormalities suggesting coronary artery disease (CAD), significant valve dysfunction > grades I.
- •8) Coronary artery disease, defined by a history of myocardial infarction, known coronary stenosis > 70% detected either by angiography or by CT-scan, significant defects in myocardial scintigraphy or positive stress-test echocardiography.
- •9) A disease other than diabetes lowering the patient’s life expectancy to less than two years.
- •10) Chronic infections or malignancies.
- •11) Systemic treatment with corticosteroids.
- •12) Renal replacement therapy.
- •13) Women of child-bearing potential (WOCBP), defined as all women physiologically
- •capable of becoming pregnant, including women whose career, lifestyle, or sexual
- •orientation precludes intercourse with a male partner and women whose partners have
- •been sterilized by vasectomy or other means, UNLESS they meet the following definition of post-menopausal: 12 months of natural (spontaneous) amenorrhea or 6 months of spontaneous amenorrhea with serum Follicle Stimulating Hormone (FSH) levels >40mIU/m or 6 weeks post surgical bilateral oophorectomy with or without hysterectomy OR are using one or more of the following acceptable methods of contraception: surgical sterilization (e.g., bilateral tubal ligation), hormonal contraception (implantable, patch, and oral), and double-barrier methods (if accepted by local regulatory authority and ethics committee). Reliable contraception should be maintained throughout the study and for 7 days after study drug discontinuation.
- •14) Pregnant or nursing (lactating) women, where pregnancy is defined as the state of a female after conception and until the termination of gestation, confirmed by a positive Human Chorionic Gonadotropin (hCG) laboratory test ( > 5mIU/ml).
- •15) History of noncompliance to medical regimes and patients who are considered
- •potentially unreliable.
- •16) Current double blind treatment in diabetic trials.
- •17) Participation in an investigational drug study at the time of enrollment or within the past 90 days.
研究者
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T-proBNP Selected PreventiOn of cardiac eveNts in a populaTion of dIabetic patients without A history of Cardiac disease a prospective randomized trial<br>diabetes cardiac disease10012653diabetes mellitusNL-OMON47526Medical university of Vienna200
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尚未招募
Unknown
Evaluation of NT-ProBNP marker to predict the cardiovascular risk in individuals with type 2 diabetes.CTRI/2023/12/060795Roche Diagnostics
