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

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

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00997165
Acronym
NUMEVOX
Enrollment
500
Registered
2009-10-19
Start date
2008-03-31
Completion date
2017-03-31
Last updated
2009-10-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Atherosclerosis, Metabolic Diseases, Sleep Apnea

Keywords

fatty liver, adipose tissue

Brief 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.

Interventions

None listed

Sponsors

University Hospital, Angers
Lead SponsorOTHER_GOV

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

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)

Countries

France

Contacts

Primary ContactPIERRE HENRI DUCLUZEAU, MD PhD
phducluzeau@chu-angers.fr33(0)663384160
Backup ContactGEORGES LEFTHERIOTIS, MD-PHD
geleftheriotis@chu-angers.fr33(2)41-35-44-56

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026