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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COMPLETED
250 participants
OBSERVATIONAL
2008-08-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
CROSS_SECTIONAL
Study Groups
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Breast cancer
Diagnosed with breast cancer 1/1/2003 - 31/12/2007.
Fasting blood sample.
Fasting blood sample taken following informed consent for genotyping, glucose and insulin levels.
Interventions
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Fasting blood sample.
Fasting blood sample taken following informed consent for genotyping, glucose and insulin levels.
Eligibility Criteria
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Inclusion Criteria
* Diagnosed with breast cancer between 1/1/2003 and 31/12/2007.
* Able to understand and willing to sign informed consent.
Exclusion Criteria
* Known diagnosis of inflammatory bowel disease or malabsorption syndrome.
* Known diagnosis of endocrine problems associated with the development of obesity (cushings syndrome, hypo/hyperthyroid, thyroiditis)
* Treatment for psychiatric disorders.
18 Years
FEMALE
No
Sponsors
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The Royal Bournemouth Hospital
OTHER
Responsible Party
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Principal Investigators
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Tamas Hickish
Role: PRINCIPAL_INVESTIGATOR
Royal Bournemouth and Christchurch Hospitals NHS Foundation Trust
Other Identifiers
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08/H0201/35
Identifier Type: -
Identifier Source: org_study_id
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