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NCT00997165 Clinical Trial

Impact of Adipose Tissue Repartition on the Time Course of Vascular Dysfunction - the NUMEVOX Cohort

Atherosclerosis Clinical Trial

— NUMEVOX  

Official title:
Impact of Adipose Tissue Repartition on the Time Course of Vascular Dysfunction - the NUMEVOX Cohort

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT00997165
Other study ID # CHU-Promoteur 08-01
Secondary ID
Status Recruiting
Phase N/A
First received October 16, 2009
Last updated October 16, 2009
Start date March 2008
Est. completion date March 2017

Study information
Verified date October 2009
Source University Hospital, Angers
Contact PIERRE HENRI DUCLUZEAU, MD PhD
Phone 33(0)663384160
Email phducluzeau@chu-angers.fr
Is FDA regulated No
Health authority France: Ministry of Health
Study type Observational

Clinical Trial Summary

The NUMEVOX cohort is intended to follow-up the macro and microvascular dysfunction in relation to adipose tissue repartition in patients with metabolic syndrome associated to liver steatosis, sleep apnea. Duration of the follow-up is 3 years for each patient entering the cohort.

Recruitment information / eligibility
Status Recruiting
Enrollment 500
Est. completion date March 2017
Est. primary completion date March 2014
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria:

- informed consent

- age > 18 years old

- suspected of metabolic syndrome

- affiliated to french social health care

Exclusion Criteria:

- age < 18 years old

- pregnancy

- no informed consent

- not eligible for the study (no MS, cancer)

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

Locations
Country Name City State
France Pôle Maladies Métaboliques et Médecine Interne Angers

Sponsors (1)
Lead Sponsor Collaborator
University Hospital, Angers

Country where clinical trial is conducted

France, 

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