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临床试验/NCT02462746
NCT02462746已完成1 期

The Effect of Cysteine, Tryptophan and Tyrosine Supplements on Breast Milk

Centre for Addiction and Mental Health2 个研究点 分布在 1 个国家目标入组 24 人开始时间: 2015年3月最近更新:
适应症

试验速览

阶段
1 期
状态
已完成
入组人数
24
试验地点
2
主要终点
Breast milk cysteine levels

研究概览

简要总结

The purpose of this project is to study the effect of dietary supplementation with a natural health product (NHP) with a focus on its effects on its levels in breast milk.

详细描述

The effect of oral cysteine on its levels in breast milk and plasma will be measured in breast feeding mothers.

The investigators will not be studying tryptophan and tyrosine in this study. The title is an overview title left over from other past studies (but the investigators are only assessing cysteine at this time).

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
None

入排标准

年龄范围
18 Years 至 45 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • Subjects would be healthy mothers who are breastfeeding at the moment, but plan to stop at the time of study
  • The subject, as reported, should be in a good health
  • The subject is not taking any medication
  • The subject is not taking any investigational medicinal product within 8 weeks prior to dosing
  • The subject does not have any known hypersensitivity to components in the proposed treatment
  • The subject does not have a history of severe drug allergy or drug hypersensitivity
  • Other general medical requirements for inclusion:
  • Age 18 to 45
  • BMI 19 to 40 (kg/m2)
  • Resting pulse between 45 and 100 bpm
  • Systolic blood pressure between 91 and 139 mmHg (inclusive)
  • Diastolic blood pressure between 51 and 90 mmHg (inclusive)
  • Orthostatic blood pressure change <20 mmHg (based on the difference between supine and standing (1 minute) systolic blood pressure)
  • The subject is in good health based on their report and answer to general health questionnaire

排除标准

  • The subject has taken any investigational medicinal product within 8 weeks prior to dosing
  • The subject is pregnant (based upon urine pregnancy test at time of screening and day of supplement intake)
  • The subject has known hypersensitivity to components in the proposed treatment or to related compounds
  • The subject has a history of severe drug allergy or drug hypersensitivity involving an anaphylactic reaction i.e. shortness of breath and/or reduced blood pressure
  • Subjects who are smoking more than one package of cigarette per day will be excluded from the study
  • The subject decides to breastfeed the infant on the study day

结局指标

主要结局

Breast milk cysteine levels

时间窗: The main protocol occurs of 10 hours of time when the pharmacokinetics of the amino acid are measured.

measurement of amino acid before and after acute administration over a 10 hour period * The first visit would be the screening visit, which the subjects will be evaluated for general health status through a standardized health questionnaire. A urine test will be done in order to screen for any drug use. * On the second visit, each subject would be tested for plasma levels of the amino acid during the day. In addition breast milk will be tested in order to examine the effect of these supplements on the amino acid contents of the breast milk at few time points on both days.

次要结局

  • plasma cysteine levels(These are sampled over 10 hours before and after administration of cysteine)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Jeff Meyer

Canada Research Chair

Centre for Addiction and Mental Health

研究点 (2)

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