跳至主要内容
临床试验/NL-OMON53253
NL-OMON53253尚未招募不适用

Assessment of Mass Balance of Orally Administered [14C] Tagatose in Healthy Volunteers Using a Microtracer Approach - TrueCal

Wageningen Universiteit0 个研究点目标入组 8 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
入组人数
8

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 至 64(—)

入选标准

  • - 18-65 years old healthy female and male using contraception during and for 3
  • months after the study
  • - BMI 18.5-25 kg/m2
  • - Must be willing and able to communicate and participate in the whole study,
  • including consumption of tagatose and meals offered during study conduct
  • - Must have regular bowel movements (i.e. average stool production of >=1 and <=3
  • stools per day)Must usually eat 3 meals per day (i.e. breakfast, lunch and

排除标准

  • - Diabetes (Type 1, Type 2, or genetic form of diabetes) - Any diagnosed
  • cardiovascular (heart) disease or high blood pressure (>=140 mmHg systolic
  • and/or >=90 mmHg diastolic) - History of clinically significant cardiovascular,
  • renal, hepatic, chronic respiratory or gastro-intestinal disease,
  • immunodeficiency, endocrine, neurological or psychiatric disorders - Any
  • diagnosed respiratory disease, such as COPD or asthma - Any previous motor
  • disorders or disorders in muscle and/or lipid metabolism - Known severe kidney
  • problems - Presence of an ulcer in the stomach or gut and/or strong history of
  • indigestion - Recent or chronic history of diarrhoea - Known anaemia - A
  • personal or family history of thrombosis (clots), epilepsy, seizures, or
  • schizophrenia. - Regular use of dietary supplements (>3 times per week) -
  • Chronic use of any prescribed or over the counter pharmaceuticals (excluding
  • oral contraceptives and contraceptive devices)History of any drug or alcohol
  • abuse in the past two years - A confirmed positive alcohol breath test at
  • screening or admission - Drug use - Claustrophobia - Subjects who are on a
  • weight loss diet or following a high calorific/high protein diet in order to
  • gain weight - Subjects with functional constipation - Any known food allergies
  • or intolerances to the 14 major food allergens (celery, cereals containing
  • gluten, crustaceans, eggs, fish, lupin, milk, molluscs, mustard, tree nuts,
  • peanuts, sesame seeds, soybeans, sulphur dioxide and sulphites) or history of a
  • malabsorption syndrome including coeliac disease - Subjects who have regular
  • gastrointestinal complaints including abdominal pain, stomach upsets and
  • borborygmi or known or suspected irritable bowel syndrome - Currently taking
  • part in other scientific research - Having received a product with 14C in the
  • past 12 months - Pregnant or breastfeeding - Smoking or having used
  • nicotin-containing products in the 6 months prior to the study. - Subjects who
  • have taken antibiotics within the 60 days prior to the adaptation period. -
  • Currently involved in a structured progressive resistance training programme
  • (>3 times per week) - Sedentary lifestyle as assessed using the International
  • Physical Activity Questionnaire [IPAQ]. - Employed or undertaking a thesis or
  • internship at the department of Human and Animal Physiology - Unable to give

研究者

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