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OpenTrials
Completed

NCT Number: NCT02704260

Genetic of SportS Induced Endofibrotic Remodeling

search for a genetic cause of vascular endofibrose

Completed

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Key information

Conditions

Genetic Syndrome Congenital, Hereditary, and Neonatal Diseases and Abnormalities Genetic Diseases, Inborn

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University Hospital

Angers, 49933, France

About this study

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

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Genetic analysis

Genetic

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

Primary outcomes

  1. Presence of mutations or nucleotides variations

    Time frame: 1 hour

    DNA analysis and search for genetic mutations

Sponsors and collaborators

Lead sponsor

University Hospital, Angers

Other Gov

Registry information

Official study title

Endofibrose Vasculaire et génétique

Acronym: GOSSER

Important dates

Study start
2016
Primary completion
2016
Study completion
2016
First posted
Mar 9, 2016
Registry last updated
Nov 1, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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