The Effect of Sleeve Gastrectomy on Food Preference (FPQ)
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| ClinicalTrials.gov Identifier: NCT02124993 |
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Recruitment Status :
Completed
First Posted : April 29, 2014
Last Update Posted : January 11, 2016
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| Condition or disease | Intervention/treatment |
|---|---|
| Severe Obesity | Other: Questionnaire |
| Study Type : | Observational |
| Actual Enrollment : | 15 participants |
| Time Perspective: | Prospective |
| Official Title: | The Effect of Sleeve Gastrectomy on Food Preference |
| Study Start Date : | April 2013 |
| Actual Primary Completion Date : | June 2014 |
| Actual Study Completion Date : | September 2015 |
| Group/Cohort | Intervention/treatment |
|---|---|
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Sleeve gastrectomy surgery Participants
Male or female who will undergo a sleeve gastrectomy for obesity by Dr. Drake Bellanger.
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Other: Questionnaire
Dr. Ballanger's office will administer a FPQ upon approval of an informed consent. Subjects will be asked to complete the questionnaire at a pre-operative visit and six weeks post-operatively.
Other Name: Food Preference questionnaire (FPQ) |
- Participants food preferences before sleeve gastrectomy surgery and after surgery. [ Time Frame: Change from Baseline in preferences after follow-up six weeks ]A list of food items are on a questionnaire asking food preferences, Breads, Cereals, Grain products, Fruits and Juices, Fats and oils, Milk, etc. which allows the subjects to select their food preferences before and after the surgery.
- Participants weight change before sleeve gastrectomy surgery and after surgery focusing on specific macronutrient. [ Time Frame: Change from Baseline in weight after follow-up six weeks ]A participant is weighted at baseline visit and follow-up visit 6 weeks after the surgery.
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| Ages Eligible for Study: | 18 Years and older (Adult, Older Adult) |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | No |
| Sampling Method: | Non-Probability Sample |
Inclusion Criteria:
- Male or Female, 18 years or over, who will undergo a sleeve gastrectomy for obesity by Dr. Drake Bellanger.
Exclusion Criteria:
- Women who are pregnant or nursing.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02124993
| United States, Louisiana | |
| Dr. Drake Bellanger | |
| Baton Rouge, Louisiana, United States, 70817 | |
| Principal Investigator: | Frank Greenway, MD | Pennington Biomedical Research Center |
| Responsible Party: | Frank Greenway, Principal Investigator, Pennington Biomedical Research Center |
| ClinicalTrials.gov Identifier: | NCT02124993 |
| Other Study ID Numbers: |
PBRC 13029 |
| First Posted: | April 29, 2014 Key Record Dates |
| Last Update Posted: | January 11, 2016 |
| Last Verified: | January 2016 |
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Gastrectomy |
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Obesity, Morbid Obesity Overnutrition |
Nutrition Disorders Overweight Body Weight |

