Study Results
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View full resultsBasic Information
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COMPLETED
34 participants
OBSERVATIONAL
2017-12-15
2021-09-30
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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Gastric bypass
Obese patients due to undergo gastric bypass surgery
Food Preference
Buffet meal to assess food preference
Control
Healthy free-living individuals
Food Preference
Buffet meal to assess food preference
Interventions
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Food Preference
Buffet meal to assess food preference
Eligibility Criteria
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Inclusion Criteria
A) Bariatric surgery B) Controls with no history of bariatric surgery
2. Independently mobile
3. Capacity to consent to participate
4. \>18 years of age
Exclusion Criteria
2. Post-operatively: significant and persistent surgical complications or anything that prevents subjects from eating a meal.
3. Systemic or gastrointestinal condition which may affect food intake or preference, including:
i) pregnancy or ii) breast feeding.
4. Active and significant psychiatric illness including substance misuse
5. Significant cognitive or communication issues
6. Medications with documented effect on food intake or food preference
7. History of significant food allergy and certain dietary restrictions
8. History of liver disease or pancreatitis
9. History of bradyarrythmia or congestive cardiac failure group)
10. Use of medications with potential serious interactions with Octreotide
18 Years
ALL
Yes
Sponsors
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Imperial College London
OTHER
Responsible Party
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Carel Le Roux
Reader in Investigative Science
Principal Investigators
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Carel le Roux, MBChB, PhD
Role: PRINCIPAL_INVESTIGATOR
Imperial College London
Locations
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University College Dublin
Dublin, , Ireland
Countries
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Provided Documents
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Document Type: Study Protocol and Statistical Analysis Plan
Document Type: Informed Consent Form
Other Identifiers
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GutHormoneStudy
Identifier Type: -
Identifier Source: org_study_id
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