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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03259997
Other study ID # ProFormance135
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date August 14, 2017
Est. completion date May 9, 2018

Study information

Verified date March 2019
Source Probi AB
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Efficacy of probiotics on physical performance


Recruitment information / eligibility

Status Completed
Enrollment 53
Est. completion date May 9, 2018
Est. primary completion date May 9, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 40 Years
Eligibility 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)

Study Design


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
Probiotic supplement
Probiotic supplement
Placebo
Placebo

Locations

Country Name City State
Sweden Idrottsmedicinska enheten, Umeå universitet Umeå

Sponsors (1)

Lead Sponsor Collaborator
Probi AB

Country where clinical trial is conducted

Sweden, 

Outcome

Type Measure Description Time frame Safety issue
Primary Metabolic response at standardized workloads during ergometer cycling Change from baseline in metabolic response at standardized workloads during ergometer cycling after 4,8 and 12 weeks of supplementation 4,8 and 12 weeks
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