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

U

University Hospital, Angers

Status

Unknown

Conditions

Metabolic Diseases
Sleep Apnea
Atherosclerosis

Study type

Observational

Funder types

Other

Identifiers

NCT00997165
CHU-Promoteur 08-01

Details and patient eligibility

About

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.

Enrollment

500 estimated patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

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)

Trial design

500 participants in 3 patient groups

Metabolic syndrome (MS)
Description:
Patients suspected of metabolic syndrome without sleep apnea or liver steatosis
MS with sleep apnea
Description:
Metabolic syndrome with sleep apnea
MS with Liver steatosis
Description:
Metabolic syndrome with liver steatosis

Trial contacts and locations

1

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Central trial contact

GEORGES LEFTHERIOTIS, MD-PHD; PIERRE HENRI DUCLUZEAU, MD PhD

Data sourced from clinicaltrials.gov

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