NCT02679248终止2 期
A Double Blind, Placebo Controlled Parallel Study to Investigate the Effect of a Nitric Oxide Supplementation Product on Pre- and Mildly Hypertensive Adults.
适应症
干预措施
试验速览
- 阶段
- 2 期
- 状态
- 终止
- 入组人数
- 67
- 试验地点
- 4
- 主要终点
- Daytime Systolic BP
研究概览
简要总结
This study will investigate the effect of a nitric oxide supplementation product, Neo40 Daily®, on blood pressure in pre-hypertensive and mildly hypertensive adults. Subjects will take 2 lozenges per day 12 hours apart for 8 weeks. Half of the subjects will receive Neo40 Daily® and the other half of the subjects will receive placebo.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Other
- 盲法
- Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
入排标准
- 年龄范围
- 18 Years 至 65 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •If female, subject is not of child bearing potential, which is defined as females who have had a hysterectomy or oophorectomy, bilateral tubal ligation or are post-menopausal (natural or surgically with > 1 year since last menstruation) OR Females of childbearing potential must agree to use a medically approved method of birth control and have a negative urine pregnancy test result. Acceptable methods of birth control include:
- •Hormonal contraceptives including oral contraceptives, hormone birth control patch (Ortho Evra), vaginal contraceptive ring (NuvaRing), injectable contraceptives (Depo-Provera, Lunelle), or hormone implant (Norplant System)
- •Double-barrier method
- •Non-hormonal intrauterine devices
- •Vasectomy of partner
- •BMI 18.5-29.9 kg/m2 (±1 kg/m2)
- •Seated resting systolic blood pressures between 130-150 mmHg (inclusive) and diastolic blood pressure ≤ 100 mmHg at screening visit
- •Agreement to maintain current level of physical activity and diet throughout the study
- •Agrees to comply with study procedures including willingness to fast at least 12 hours before blood samples, abstain from alcohol two days prior to blood sampling and blood pressure measurement, abstain from coffee at least 14 hours before blood pressure measurement and abstain from physical exercise at least 4 hours before and during blood pressure measurement
- •Has given voluntary, written, informed consent to participate in the study
排除标准
- •Has given voluntary, written, informed consent to participate in the study
- •Use of medication for the treatment of hypertension
- •Use of prescription diuretics
- •Use of natural health products for the treatment of hypertension within 2 weeks of screening (e.g. garlic supplements, french lavender supplements, cardamom supplements, cinnamon supplements, basil supplements, hawthorn cats claw and celery seed supplements)
- •Significant cardiac history defined as a history of myocardial infarction (MI); coronary angioplasty or bypass graft(s); Valvular disease or repair; unstable angina pectoris; transient ischemic attack (TIA); cerebrovascular accidents (CVA); congestive heart failure; coronary artery disease (CAD); or angina (stable or unstable)
- •Type I or Type II diabetes
- •Diagnosis of hypertensive retinopathy, left ventricular dysfunction or peripheral artery disease
- •Abnormal electrolytes, liver or kidney function
- •Diagnosis of secondary hypertension
- •Diagnosis of anemia
- •Unstable medical conditions that in the opinion of the Qualified Investigator preclude the volunteer from participating in the study
- •Alcohol or drug abuse within the last 6 months
- •Use of medicinal marijuana
- •Clinically significant abnormal laboratory results at screening
- •Participation in a clinical research trial within 30 days prior to randomization
- •Allergy or sensitivity to study supplement ingredients
- •Individuals who are cognitively impaired and/or who are unable to give informed consent
- •Any other condition which in the Investigator's opinion may adversely affect the subject's ability to complete the study or its measures or which may pose significant risk to the subject
研究组 & 干预措施
Neo40 Daily®
Experimental
干预措施: Neo40 Daily® (Dietary Supplement)
Placebo
Experimental
干预措施: Placebo (Dietary Supplement)
结局指标
主要结局
Daytime Systolic BP
时间窗: 8 weeks
Mean ambulatory BP measured from 8am to 8pm
次要结局
- Seated BP(8 weeks)
- 24-hour BP(8 weeks)
- Serum Assay: Lipid Profile(8 weeks)
- Daytime Diastolic BP(8 weeks)
- Night-time BP(8 weeks)
- BP Variability(8 weeks)
- Serum or Plasma Assay: Inflammatory Markers(8 weeks)
研究者
研究点 (4)
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