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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT02618005
Other study ID # Probiotics
Secondary ID
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date October 2015
Est. completion date March 2023

Study information

Verified date August 2021
Source Yakult Honsha Co., LTD
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Human immune function and intestinal microbiota are suggested to be altered within long-duration stay in space. Accumulated evidences on earth support that Lactobacillus casei strain Shirota (LcS) is a promising probiotic strain on improvement of immune function and intestinal microbiota. This study aims to investigate the impact of long-duration spaceflight as well as intake of LcS on the international space station (ISS), on immune system and intestinal microbiota in astronauts.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 10
Est. completion date March 2023
Est. primary completion date March 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 25 Years to 80 Years
Eligibility Inclusion Criteria: - Individuals who are scheduled to stay on the ISS for at least 3 months - Individuals who fully understand the study protocol and provide written informed consent for the study participation Exclusion Criteria: - Individuals who routinely use antibiotic, laxative, and/or bowel regulating medicine - Individuals who participate in other research that competes with this study in terms of the purpose and field, e.g., study with dietary management or intake of bifidobacteria/lactic acid bacteria, oligosaccharides, antibiotic, laxative, and/or bowel regulating medicine

Study Design


Related Conditions & MeSH terms

  • Immune Function and Intestinal Microbiota

Intervention

Dietary Supplement:
Probiotic capsule
Continuously take five capsules containing freeze-dried LcS on ISS for four weeks, from four weeks before the return (R-4W) to one day before the return (R-1d)

Locations

Country Name City State
Japan Japan Aerospace Exploration Agency Ibaraki

Sponsors (2)

Lead Sponsor Collaborator
Yakult Honsha Co., LTD Japan Aerospace Exploration Agency

Country where clinical trial is conducted

Japan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Longitudinal changes in the number of LcS in feces Number of LcS in feces will be assessed by PMA-qPCR, during pre-flight, in-flight and post-flight. 9-18 months
Primary Longitudinal changes in the level of immune markers Levels of immune markers in blood/saliva will be assessed by ELISA and bioassay, during pre-flight, in-flight and post-flight. 9-18 months
Primary Longitudinal changes in numbers and composition of intestinal microbiota Numbers and composition of bacteria in feces will be assessed by RT-qPCR/qPCR and next generation sequencer analysis, during pre-flight, in-flight and post-flight. 9-18 months