Obesity Clinical Trial
— MUSCAADEOfficial title:
Pilot Study of Branched Amino Acid Supplementation for Patients With an Excessive Loss of Muscular Body Mass After Obesity Surgery.
Verified date | April 2019 |
Source | University Hospital, Toulouse |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Despite the demonstrable health and quality of life benefits, there are unknowns within
consequences of obesity surgery. Weight loss composition is poorly understood. The objective
is to have a significant loss of body fat and a limited loss of muscular weight.
A cohort study in the nutrition unit at Toulouse University Hospital shows that 3 months and
1 year after surgery, there are 2 phenotypes of patients. The first one is called 'little
loss' and is defined by a contribution of muscular weight lower than 15% of the total weight
loss. The other one is called 'big loss' and is defined by a contribution of muscular weight
higher than 15% of the total weight loss. Causes of these different phenotypes are unknown
for the moment.
Some amino acids have an anabolic potential. Leucine induces a muscular protein synthesis in
clinical situations like hepatic cirrhosis, and some populations like new born and older
people.
Assuming that, a leucine-enriched essential amino acid supplementation will have a benefit
effect on the muscular mass. That is testing the influence of the quality of protein
consumed, more than the quantity. An anabolic substance (amino acid here) can lead to gain of
muscle only if it is associated to regular physical training, all patients will follow a
physical training.
Status | Terminated |
Enrollment | 6 |
Est. completion date | July 13, 2017 |
Est. primary completion date | July 13, 2017 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 65 Years |
Eligibility |
Inclusion Criteria: - Patient older than 18 years of age and younger than 65 years of age, - Patient received an obesity-surgery (gastric bypass or sleeve gastrectomy) - Contribution of muscular weight higher than 15% of the total weight loss after the third month post-surgery. - Patient that be able to increase their physical activity - Patient that give their informed consent before any procedure for the study - Patient affiliated with a health insurance scheme Exclusion Criteria: - Patients allergic to one of the supplement's compound. - Patients with glucocorticoid therapy - Patients with hyperthyroidism - Patients commencing insulin treatment or growth hormone - Protein powder intake (as nutritional complement or as anabolic substance for muscle building practice) - Oral nutritional supplement intake for malnutrition - Bone fracture since the surgery - Infection can cause hypercatabolism (like microbial outbreak or chronic gastric fistula) - Hospitalization for more than 24 hours since the surgery - Known physical handicap - Inability to increase physical activity during 3 months after beginning of the supplementation - Enteral or parenteral nutrition - Patients over 158 kg (DEXA impossible) - Protected adults (guardianship by court order) - Pregnant woman or breastfeeding. |
Country | Name | City | State |
---|---|---|---|
France | Department of Endocrinology, metabolic diseases and nutrition | Toulouse |
Lead Sponsor | Collaborator |
---|---|
University Hospital, Toulouse |
France,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change from baseline in appendicular muscular mass at 3 months | Appendicular muscular mass measured by dual-energy X-ray absorptiometry (DEXA). It will be measured before and 3 months after supplementation. | Baseline and 3 months | |
Secondary | Change from baseline in limbs muscular force at 3 months | The lower and higher limbs muscular force will be measured with a strain gauge. | Baseline and 3 months | |
Secondary | Change from baseline in muscular function at 3 months | 400 meters walking speed | Baseline and 3 months | |
Secondary | Change from baseline in muscular function at 3 months | Chair-stand test | Baseline and 3 months | |
Secondary | Change from baseline in muscular function at 3 months | Balance test by the Short Physical Performance Battery test | Baseline and 3 months | |
Secondary | Change from baseline in fatigue at 3 months | Fatigue will be evaluate by the Pichot scale | Baseline and 3 months | |
Secondary | Change from baseline in general functional assessment at 3 months | General function will be assessed by the Functional Status Questionnaire test. | Baseline and 3 months | |
Secondary | Change from baseline in protein daily intake at 3 months | Patient will evaluate his/her protein daily intake (in g/day) by the Protein Intake Monitor with a digital tablet | Baseline and 3 months | |
Secondary | Change from baseline in physical training adhesion at 3 months | Patients will have an exercise diary to write their organised physical activity. Physical activity will be converted in a multiple of basal metabolic rate. | Baseline and 3 months | |
Secondary | Change from baseline in glucose metabolism at 3 months | Oral glucose tolerance test will be performed and glucose concentration will be determined into the blood. | Baseline and 3 months | |
Secondary | Change from baseline in insulin secretion at 3 months | Oral glucose tolerance test will be performed and insulin concentration will be determined into the blood. | Baseline and 3 months | |
Secondary | Change from baseline in leucine compliance | Leucine concentration and variation between visit before and after 3 months of supplementation will be measured by chromatography to assess the patient's compliance | Baseline and 3 months |
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