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Tolerance and Prebiotic Activity of Arabinoxylan-Oligosaccharides in Healthy Subjects

C

Catholic University (KU) of Leuven

Status and phase

Completed
Phase 4

Conditions

Healthy

Treatments

Dietary Supplement: arabinoxylan-oligosaccharides (AXOS)

Study type

Interventional

Funder types

Other

Identifiers

NCT00852813
AXOS 002

Details and patient eligibility

About

The purpose of the study is to evaluate the tolerance of a higher dose of arabinoxylan-oligosaccharides (AXOS) and their prebiotic activity in healthy subjects.

Enrollment

20 patients

Sex

All

Ages

18 to 45 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • healthy
  • 18-45 years
  • regular eating pattern

Exclusion criteria

  • gastrointestinal complaints
  • antibiotic intake
  • medication influencing gut transit or microbiota
  • abdominal surgery
  • pregnancy

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Single Blind

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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