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Role of the Renin Angiotensin Aldosterone System in the Mechanisms of Transition to Heart Failure in Abdominal Obesity (R2C2-II)

C

Central Hospital, Nancy, France

Status

Completed

Conditions

Obesity, Abdominal

Treatments

Other: Blood sample
Other: Echotracking
Other: Pulse wave velocity
Other: Glucose tolerance test
Other: cardiac and abdominal magnetic resonance imaging
Other: Assessment of sleep apnea syndrome
Other: Urine sample
Other: Composition of body mass by Dual x-ray absorptiometry
Other: Ambulatory blood pressure monitoring
Other: Electrocardiogram
Other: Echocardiography

Study type

Interventional

Funder types

Other

Identifiers

NCT01716819
2012-A00574-39

Details and patient eligibility

About

R2C2 study has shown that abdominal obesity is associated with a cardiac and vascular remodelling in healthy volunteers. This remodelling is correlated with renin-angiotensin aldosterone system (RAAS) activation and/or systemic fibrosis. R2C2 II study is designed to confirm the hypothesis that RAAS is associated with an early remodelling and implicated in the transition to cardiac failure in abdominal obesity.

Full description

Follow up of abdominal obesity patients from the R2C2 cohort study.

Enrollment

101 patients

Sex

All

Ages

43 to 72 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Being a former member of R2C2 study, abdominal obese group.
  • Having signed the informed consent (refusing to participate to the genetic study is not an exclusion criteria).
  • being affiliated to health insurance scheme.

Inclusion Criteria of R2C2 study:

  • Men and women aged between 40 and 65 year's old
  • Caucasian
  • Born or living in France for at least 10 years
  • Presenting an abdominal obesity defined by a waist circumference >94 cm in men and ≥ 80 cm in women, associated or not with untreated hypertension or hypertension treated for less than one year
  • Having signed the informed consent

Exclusion criteria

  • Subjects unable to understand the information letter
  • Subjects under supervision or guardianship
  • pregnant or lactating woman
  • A contraindication to perform MRI is not an exclusion criteria.

Trial design

101 participants in 1 patient group

Abdominal obesity
Other group
Description:
Single arm, follow up cohort in patient with abdominal obesity. No comparator: description of interventions : Composition of body mass by Dual x-ray absorptiometry Pulse wave velocity Electrocardiogram Urine sample Blood sample (and biological collection) Assessment of sleep apnea syndrome Glucose tolerance test Echocardiography Echotracking cardiac and abdominal magnetic resonance imaging Ambulatory blood pressure monitoring
Treatment:
Other: Glucose tolerance test
Other: cardiac and abdominal magnetic resonance imaging
Other: Electrocardiogram
Other: Echocardiography
Other: Pulse wave velocity
Other: Blood sample
Other: Echotracking
Other: Ambulatory blood pressure monitoring
Other: Composition of body mass by Dual x-ray absorptiometry
Other: Assessment of sleep apnea syndrome
Other: Urine sample

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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