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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02517190
Other study ID # 12-024
Secondary ID
Status Completed
Phase N/A
First received July 23, 2015
Last updated August 5, 2015
Start date May 2012
Est. completion date January 2014

Study information

Verified date August 2015
Source University Hospital, Caen
Contact n/a
Is FDA regulated No
Health authority France: Agence Nationale de Sécurité du Médicament et des produits de santé
Study type Interventional

Clinical Trial Summary

From previous parabolic flight campaigns completed by our research group investigators gathered data showing important changes in neuro‐endocrine and also immunological changes. This experiment now will complete the data set‐up obtained during the MARS500 study on how these respective individuals will re‐act to highly physically and emotionally challenging situations during a parabolic flight.

This add‐on experiment to MARS500 will enable answering to the following questions i) if the stress response systems - when compared for two conditions but in the same individuals - do react uniformly and ii) if those subjects prone to have adequate stress response pattern will show gradually less immune modulation effects.

The understanding of the complex interactions of stress and immunity under chronic and acute stress conditions might help to enable adequate health and immune monitoring and might as well suggest suitable countermeasures for the prevention of the unwanted immunological effects during long‐term confinement and space missions.


Recruitment information / eligibility

Status Completed
Enrollment 6
Est. completion date January 2014
Est. primary completion date January 2014
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- Healthy volunteers (men or women)

- Aged from 18 to 65

- Affiliated to a Social Security system and, for non-French resident, holding a European Health Insurance Card (EHIC)

- Who accepted to take part in the study

- Who have given their written stated consent

- Who participated in the MARS500 experiment

- Who has passed a medical examination similar to a standard aviation medical examination for private pilot aptitude. There will be no additional test performed for subject selection.

Exclusion Criteria:

- Person who took part in a previous biomedical research protocol, of which exclusion period is not terminated

- Pregnant women

Study Design

Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Basic Science


Related Conditions & MeSH terms


Intervention

Other:
Parabolic flight

neuro-endocrine measurements
psychic stress tests, stress hormones: prolactin, cortisol, endo-cannabinoids
immunological measurements
blood cell counts, B2 integrins, cytokines, C-reactive protein
cellular energy metabolism measurements
purines, lactate

Locations

Country Name City State
France Umr Ucbn/Inserm U1075 Comete Caen CEDEX Basse-Normandie

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Caen

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary neuro-endocrine measurements composite prolactin, cortisol, endo-cannabinoids baseline No
Primary immunological measurements composite blood cell counts, B2 integrins, cytokines, C-reactive protein baseline No
Primary cellular energy metabolism measurements composite purines, lactate baseline No
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