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The time trial performance of different food products in healthy volunteers.

Withdrawn
Conditions
n.v.t.
n/a
Registration Number
NL-OMON40549
Lead Sponsor
niversiteit Maastricht
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Withdrawn
Sex
Not specified
Target Recruitment
12
Inclusion Criteria

• Males
• Aged 18-50 years
• Blood pressure: diastolic blood pressure between 60 and 90 mmHg and a systolic
blood pressure between 100 and 150 mmHg
• Body Mass Index (BMI; weight/length2) between 18 and 25 kg/m2
• Protein and glucose are not allowed to be present in urine that will be collected
during screening.
• Subjects have to be healthy (self reported) and are not allowed to use medication
that can interfere with the current study.
• Normal Dutch dietary eating habits (no vegan, vegetarian or macrobiotic lifestyle)
• Participants must be trained cyclists / triathletes and be in possession of a positive sports examination or a competition licence.

Exclusion Criteria

• Having a history of medical or surgical events that may significantly affect the
study outcome (gastro-intestinal diseases)
• Any current metabolic or endocrine disease
• Diabetes Mellitus (type I and II)
• More than 28 consumptions of alcohol a week (for men) and more than 21 consumptions of alcohol a week (for women)
• Reported intolerance for gluten
• Having regularly gastro-intestinal complaints (stomach upsets, diarrhea, constipation, wind, abdominal colic)
• Reported unexplained weight loss or gain of >2kg in the month prior to the pre-study screening
• Reported slimming or medically prescribed diet
• Reported vegan, vegetarian or macrobiotic lifestyle
• Use of antibiotics during the last three months;• The subject will be excluded from the study if he does not want to be informed about deviating findings / accidental findings concerning his health
• The following drugs are not allowed during the study:
1. Anti-hypertensive drugs
2. Lipid lowering-drugs
3. Glucose-lowering agents.
4. Anti-inflammatory agents
5. Chronic oral or parenteral corticosteroids treatment (> 7 consecutive days of treatment).
6. Laxatives or anti-diarrhea drugs

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
<p>Cycle test (time trial) performance (time to completion of a set workload)<br /><br>after consumption of the test products (Snelle Jelle 'kruidkoek' or banana with<br /><br>water, or only water).</p><br>
Secondary Outcome Measures
NameTimeMethod
<p>N/A</p><br>
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