A study to evaluate the postprandial, short term effects of two baby nutrition products in adult, male volunteers - Postprandial effects of baby nutrition products

utricia0 个研究点目标入组 30 人开始时间: 待定最近更新: 2024年4月29日

适应症

试验速览

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•- Healthy, adult, male, Caucasian, Dutch-speaking subjects
•- Non-smokers
•- Lactose- and milk-tolerant
•- Age 18-25 yr
•- Body Mass Index (BMI) of 20-25 kg/m2
•- Girth width <100 cm
•- Stable body weight (weight gain or loss < 2 kg in the past three months)
•- Willing to give up being a blood donor (or having donated blood) from 8 weeks before the start of the study, during the study, and 4 weeks after the study (i.e. after the follow-up phone call)
•- Written informed consent

•- Top sports men or athletes with a daily strenuous training program (>2 hr)
•- Known diseases or malfunctions e.g. fat malabsorption, gastrointestinal malformations, haemophilia, hepatitis B, human immunodeficiency virus (HIV), high blood-pressure, hyperlipidaemia or diabetes
•- Current illnesses which could interfere with the study (e.g. prolonged severe diarrhoea, regurgitation, severe flu): to be determined on judgement of the investigator
•- Medication use (except for paracetamol) or a medically prescribed diet
•- More than 21 alcoholic consumptions per week
•- Use of vitamin supplements, fish oil capsules or products rich in plant stanol or sterol esters during the study and 2 weeks in advance of study start
•- Any current participation, or participation within 8 weeks before study start, in any other study involving investigational or marketed products
•- Investigator's uncertainty about the willingness or ability of the subject to comply with the protocol requirements and instructions

发起方

utricia