Genetic of SportS Induced Endofibrotic Remodeling

NCT ID: NCT02704260

Last Updated: 2017-11-01

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

Clinical Phase

NA

Total Enrollment

5 participants

Study Classification

INTERVENTIONAL

Study Start Date

2016-03-02

Study Completion Date

2016-09-02

Brief Summary

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search for a genetic cause of vascular endofibrose

Detailed Description

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Perform a DNA analysis to mark the existence of mutations in one or more genes encoding proteins involved in vascular remodeling high.

5 patients or relatives of patients topics

Conditions

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Genetic Syndrome

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

DIAGNOSTIC

Blinding Strategy

NONE

Study Groups

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GENETIC ANALISYS

GENETIC ANALYSIS AND RESEARCH OF GENETIC BLOOD SAMPLE

Group Type EXPERIMENTAL

GENETIC ANALYSIS

Intervention Type GENETIC

prélevement blood to search for a genetic cause of vascular endofibrose. Search genetic mutations in 5 subjects.

Interventions

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GENETIC ANALYSIS

prélevement blood to search for a genetic cause of vascular endofibrose. Search genetic mutations in 5 subjects.

Intervention Type GENETIC

Eligibility Criteria

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Inclusion Criteria

* High level reached Cyclists vascular endofibrose
* Cyclist high level and not sick with a brother or sister is senior cyclist reaches the vascular endofibrose.

Exclusion Criteria

* not obtaining consent
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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University Hospital, Angers

OTHER_GOV

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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PIERRE ABRAHAM, PROFESSOR

Role: PRINCIPAL_INVESTIGATOR

UH ANGERS

Locations

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University Hospital

Angers, , France

Site Status

Countries

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France

Other Identifiers

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2015-A00441-48

Identifier Type: -

Identifier Source: org_study_id