Vitamin D3 Absorption Studies in Healthy Adult Volunteers.

Medlab Clinical0 个研究点目标入组 60 人开始时间: 2016年8月3日最近更新: 2020年1月13日

适应症

试验速览

暂无简介。

•Participants >18 years of age - 80 years of age at time of entry into the study;
•1) No evidence or documented history of a chronic disease
•2) Cognitive ability to understand informed consent process and to give informed consent to the experimental treatment

•Any clinically relevant abnormal findings which, in the opinion of the investigators/clinicians, may put the participant at risk of adverse events because of participation in the clinical trial including;
•1) Previous history of abnormal blood results i.e. FBE, U and E Liver Function Tests
•2) Vital signs
•3) The use of any nicotine products including;
•i) nicotine patches/gum ii) tobacco smoking
•4) Alcohol abuse
•5) The use of any illicit drugs
•6) Unstable angina not well managed with medication
•7) Pregnancy or nursing of an infant
•8) Any psychiatric disorders by history or examination that would prevent completion of the study or result in possible adverse events for the participant [i.e. suicide thoughts or euthanasia requests]

发起方

Medlab Clinical