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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02704260
Other study ID # 2015-A00441-48
Secondary ID
Status Completed
Phase N/A
First received February 23, 2016
Last updated October 30, 2017
Start date March 2, 2016
Est. completion date September 2, 2016

Study information

Verified date December 2016
Source University Hospital, Angers
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

search for a genetic cause of vascular endofibrose


Description:

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


Recruitment information / eligibility

Status Completed
Enrollment 5
Est. completion date September 2, 2016
Est. primary completion date September 2, 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility 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

Study Design


Related Conditions & MeSH terms


Intervention

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

Locations

Country Name City State
France University Hospital Angers

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Angers

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Presence of mutations or nucleotides variations DNA analysis and search for genetic mutations 1 hour
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