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Completed

NCT Number: NCT01957098

The Effects of L-Arabinose and D-xylose on Intestinal Sucrase Activity in Man

The purpose of this study is to investigate the effect of L-arabinose and D-xylose in a sugar-rich drink on intestinal sucrase activity in healthy volunteers by measuring postprandial blood glucose and insulin, and selected intestinal hormonal responses to increasing doses of L-arabinose and D-xylose.

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Key information

Age range

18 year–30 year

Sex eligibility

Male

Study type

Interventional

Phase

Not applicable

Primary location

Institute of Human Nutrition, The Royal Veterinary and Agricultural University

Frederiksberg, DK-1958, Denmark

About this study

Based on previous scientific results we hypotesize, that pentoses decreases the demand for insulin in metabolizing a given dose of sucrose.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • healthy males
  • BMI between 18.4-25 kg/m2
  • age between 18 and 30

Exclusion criteria

  • donation of blood 3 months before or during the study
  • gastrointestinal disorders, diabetes, hypertension, hyperlipidemia, chronic infectious disease (HIV or hepatitis)
  • smoking
  • consumption of more than 21 alcoholic drinks/week
  • elite athletes
  • on medication

Treatment and study plan

Placebo comparator: 0% pentose

Dietary Supplement

14 healthy subjects participated in a randomized double-blinded cross-over study based on four single tests. Sucrose containing drinks were supplemented with two different doses of D-xylose and in addition one dose of L-arabinose was included for comparison with earlier studies. Blood was collected fasting and for 3-h postprandially. Appetite sensations and energy intake were registered. Gastrointestinal symptoms were monitored for 24 hours

Active comparator: 4% D-xylose

Dietary Supplement

Active comparator: 8% D-xylose

Dietary Supplement

Active comparator: 8% L-arabinose

Dietary Supplement

Primary outcomes

  1. Blood glucose, insulin, C-peptide and GLP-1

    Time frame: -15, 0, 15, 30, 45, 60, 90, 120, 180 min

    Level of glucose, insulin, C-peptide and glucagon-like peptide-1 (GLP-1) over time, the area under the curve (AUC), the peak value and time to peak

Secondary outcomes

  1. Appetite measurements and energy intake

    Time frame: -15, 30, 60, 90, 120, 150 and 180 min

    Appetite measurements: area under/over the curve (AUC/AOC), 3-h mean. Energy intake: the ad libitum energy intake at lunch was registered. VAS was used to asses the palatability (appearance, smell, taste, after-taste and overall palatability) of the ad libitum lunch.

Sponsors and collaborators

Lead sponsor

University of Copenhagen

Other

Collaborators

  • Danisco

Registry information

Acronym: M192

Important dates

Study start
2006
Primary completion
2007
Study completion
2007
First posted
Oct 8, 2013
Registry last updated
Oct 8, 2013

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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