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Note: This record shows only the 20 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: ClinicalTrials.gov
Last refreshed on: 17 October 2012
Main ID:  NCT01030549
Date of registration: 09/12/2009
Primary sponsor: University of Campinas, Brazil
Public title: Latin American Multicenter Cardiovascular Magnetic Resonance Reference Study
Scientific title: Latin American Multicenter Cardiovascular Magnetic Resonance Reference Study
Date of first enrolment: December 2009
Target sample size: 300
Recruitment status: Recruiting
URL:  http://clinicaltrials.gov/show/NCT01030549
Study type:  Observational
Study design:  Observational Model: Cohort, Time Perspective: Cross-Sectional  
Countries of recruitment
Brazil
Contacts
Name:   Juliano L Fernandes, MD, PhD
Address: 
Telephone: +55-19-35792903
Email: jlaraf@fcm.unicamp.br
Affiliation: 
Name:   Juliano L Fernandes, MD, PhD
Address: 
Telephone: +55-19-37592903
Email: jlaraf@fcm.unicamp.br
Affiliation: 
Name:   Juliano L Fernandes, MD, PhD
Address: 
Telephone:
Email:
Affiliation:  University of Campinas, Brazil
Key inclusion & exclusion criteria

Inclusion Criteria:

- Asymptomatic subjects with 20 to 80 years of age with no history of cardiac disease,
no known risk factors with normal physical examination and ECG

Exclusion Criteria:

- Current smokers or smokers with < 10 years of quitting

- Systolic blood pressure > 120mmHg or diastolic blood pressure > 80mmHg

- Fasting blood glucose > 100mg/dL

- Total cholesterol > 240mg/dL



Age minimum: 20 Years
Age maximum: 80 Years
Gender: Both
Health Condition(s) or Problem(s) studied
Healthy
Intervention(s)
Primary Outcome(s)
CMR data: end-diastolic volume, end-systolic volume, stroke volume, cardiac output, ejection fraction, mass, ascending and descending aortic diameters, aortic arch diameter, atrial diameter, interventricular septum thickness, posterior wall thickness. [Time Frame: At enrollment of patients (time zero). No follow-up will be performed since the trial is cross-sectional]
Secondary Outcome(s)
Secondary ID(s)
CMRLAC-01
Source(s) of Monetary Support
Please refer to primary and secondary sponsors
Secondary Sponsor(s)
Fundação de Amparo à Pesquisa do Estado de São Paulo
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