Evaluation of Biological Markers of Mesenteric Ischemia During an Ultra-trail

NCT ID: NCT03205098

Last Updated: 2017-07-02

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

200 participants

Study Classification

OBSERVATIONAL

Study Start Date

2015-06-19

Study Completion Date

2016-09-30

Brief Summary

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To assess the evolution of biological markers of mesenteric ischemia during ultratrail.

Detailed Description

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During physical exercise, increased sympathetic nervous system activity redistributes blood flow from splanchnic organs to working muscles. With prolonged duration and / or intensity, the splanchnic blood flow can be reduced by 80% or more. A severely reduced of splanchnic blood flow can frequently cause gastrointestinal ischemia. This ischemia associated with reduced vagal activity probably results in changes in motility and absorption.

High symptoms are reported in 40% of runners with reflux and heartburn in 15-20% of runners. The low symptoms have an incidence of about 70% in the long runs type ultra-trail.

Biological markers such as I-FABP have been shown to be useful in the diagnosis of mesenteric ischemia.

Conditions

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Ultra-trail Participation

Study Design

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Observational Model Type

OTHER

Study Time Perspective

PROSPECTIVE

Study Groups

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Runners

To assess the evolution of biological markers of mesenteric ischemia during ultratrail.

Blood analysis

Intervention Type BIOLOGICAL

Blood test of biological markers of mesenteric ischemia

Interventions

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Blood analysis

Blood test of biological markers of mesenteric ischemia

Intervention Type BIOLOGICAL

Eligibility Criteria

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Inclusion Criteria

* Healthy Voluntary Subject
* Age \> 18 years
* Written consent
* Subject affiliated to Social Security
* Medical certificate (mandatory to take part in the ultra-trail)

Exclusion Criteria

* Refusal to participate
* Subject with legal protection (guardianship, trusteeship)
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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University Hospital, Clermont-Ferrand

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Sébastien PERBET

Role: PRINCIPAL_INVESTIGATOR

CHU de Clermont-Ferrand

Locations

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CHU de Clermont-Ferrand

Clermont-Ferrand, Auvergne, France

Site Status

Countries

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France

Other Identifiers

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2015-A00470-49

Identifier Type: OTHER

Identifier Source: secondary_id

CHU-340

Identifier Type: -

Identifier Source: org_study_id

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