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OpenTrials
Completed

NCT Number: NCT03259997

Efficacy of Probiotics on Physical Performance

Efficacy of probiotics on physical performance

Completed

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Key information

Age range

18 year–40 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Idrottsmedicinska enheten, Umeå universitet

Umeå, 90187, Sweden

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Male or female, aged 18 to 40 years, at the time of signing the informed consent form
  • Provides signed and dated informed consent form
  • Engaged in competitive sports and regularly training
  • Non-anemic, iron-deficient
  • Willing to comply with all study procedures and be available for the duration of the study

Exclusion criteria

  • Use of probiotics
  • Use of iron supplementation
  • Use of ascorbic acid (Vitamin C) supplementation
  • Hypersensitivity to any of the ingredients in the investigational product (IP)

Treatment and study plan

Probiotic supplement

Dietary Supplement

Probiotic supplement

Placebo

Dietary Supplement

Placebo

Primary outcomes

  1. Metabolic response at standardized workloads during ergometer cycling

    Time frame: 4,8 and 12 weeks

    Change from baseline in metabolic response at standardized workloads during ergometer cycling after 4,8 and 12 weeks of supplementation

Sponsors and collaborators

Lead sponsor

Probi AB

Industry

Registry information

Important dates

Study start
2017
Primary completion
2018
Study completion
2018
First posted
Aug 24, 2017
Registry last updated
Mar 20, 2019

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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