(Mol-SHARE) Molecular Study of Health Assessment and Risk in Ethnic Groups
NCT ID: NCT00249314
Last Updated: 2007-04-19
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
120 participants
OBSERVATIONAL
2005-11-30
2007-12-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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DEFINED_POPULATION
OTHER
Eligibility Criteria
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Inclusion Criteria
* Between 18-50 years of age
* Fits into one of the following BMI-Strata:
* Stratum 1: BMI 18.5 - 25 kg/m2
* Stratum 2: BMI 25.1 -29.9 kg/m2
* Stratum 3: BMI 30 -45 kg/m2
* Ability and willingness to complete dietary and activity diaries and questionnaires
Exclusion Criteria
* Use of systemic glucocorticosteroids (topical and inhaled corticosteroids are acceptable)
* If the participant has any one or more of the following medical disorders:
* Known Diabetes
* Known renal impairment
* Known uncontrolled endocrine disorder (e.g. hyperthyroidism, Cushing's syndrome, acromegaly, etc.)
* Recent (less than three months) major surgery or hopitalization for severe illness
* History of active malignancy, chronic inflammatory disorder, or chronic infections which would interfere with the protocol completion
* Any other medical, social or geographic condition, which in the opinion of the investigator would not allow safe or reliable completion of the protocol
* Anticoagulant therapy (e.g. Coumadin)
* Orthopaedic contraindication to exercise test
* Significant fluctuations in weight over past 3 months (e.g. \>10%)
* Extreme weight loss diets (e.g. Atkins, Bernstein)
* History of drug or alcohol dependency within six months prior to signing the informed consent form
* If the participant has any contraindications to MRI:
* If the participant is clautrophobic or suffers from fear of closed spaces
* If participant has had significant contact with metal (e.g. welding)
* If participant has foreign body in their eye as confirmed by X-ray of the orbits
* Body Mass Index \> 45 kg/m2
* Participant has had hip or joint replacement surgery 6-8 weeks prior to start of study
* If participant has:
* Cardiac pacemaker
* Artificial cardiac valve
* Aneurysm clip
* Neurostimulator
* Other implanted devices or metal objects in their body
18 Years
50 Years
ALL
Yes
Sponsors
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Heart and Stroke Foundation of Canada
OTHER
Hamilton Health Sciences Corporation
OTHER
Principal Investigators
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Arya M Sharma, MD, FRCPC
Role: PRINCIPAL_INVESTIGATOR
McMaster University
Sonia Anand, MD, FRCPC
Role: PRINCIPAL_INVESTIGATOR
McMaster University
Mark Tarnopolsky, MD, FRCPC
Role: PRINCIPAL_INVESTIGATOR
McMaster University
Locations
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Hamilton Health Sciences - Cardiovascular Obesity Research and Management Center
Hamilton, Ontario, Canada
Countries
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Central Contacts
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Other Identifiers
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Mol-SHARE
Identifier Type: -
Identifier Source: org_study_id