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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RECRUITING
3600 participants
OBSERVATIONAL
2010-04-30
2037-04-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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CASE_CONTROL
PROSPECTIVE
Study Groups
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Crohn's disease patients
Diagnosis of Crohn's disease by endoscopy, radiology and histology
No interventions assigned to this group
Ulcerative colitis patients
Diagnosis of ulcerative colitis defined by endoscopy, radiology and histology
No interventions assigned to this group
Non-IBD patients
Ethically, sex and aged-matched controls attending clinics or endoscopy for functional upper gastrointestinal diseases or screening colonoscopy.
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* Informed consent given by patient or family
Case group (IBD patients) Diagnosis of Crohn's disease or ulcerative colitis defined by endoscopy, radiology and histology
Control group (non-IBD cases) Ethically, sex and aged-matched controls attending clinics or endoscopy for functional upper gastrointestinal diseases or screening colonoscopy.
Exclusion Criteria
* Controls will be excluded if they have previously been diagnosed with IBD or if they have a first or second degree relative with IBD.
18 Years
ALL
Yes
Sponsors
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Chinese University of Hong Kong
OTHER
Responsible Party
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Siew Chien NG
Professor
Principal Investigators
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Siew C NG, PhD
Role: PRINCIPAL_INVESTIGATOR
Chinese University of Hong Kong
Locations
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Prince of Wales Hospital
Hong Kong, , Hong Kong
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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IBD GWA
Identifier Type: -
Identifier Source: org_study_id
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