Healthy Volunteers Clinical Trial
Official title:
Nutritional Intervention Study to Evaluate the Effect of an Olive Oil Lipid Rich in Diglycerides as a Fat Replacement in Different Meat Products, in a Healthy Population
| Verified date | June 2016 |
| Source | IMDEA Food |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | Spain: Comité Ético de Investigación Clínica |
| Study type | Interventional |
Nutritional clinical trial to evaluate the effectiveness of different functional meat products on the nutritional status of healthy people
| Status | Completed |
| Enrollment | 78 |
| Est. completion date | June 2015 |
| Est. primary completion date | June 2015 |
| Accepts healthy volunteers | Accepts Healthy Volunteers |
| Gender | Both |
| Age group | 18 Years to 65 Years |
| Eligibility |
Inclusion Criteria: - Men and women between 18 - 65 years old. - BMI >20<27 - Adequate education level and comprehension of the clinical study. - Willingness to participate in the study as a volunteer and to provide written consent. Exclusion Criteria: - Diagnosis of Type I Diabetes . - BMI >27 - Dyslipidemia under pharmacological treatment. - High blood pressure. - Dementia, neurological disease or reduction of cognitive function. - Severe illness (hepatic disease, renal disease, etc.). - Refusal to consume the experimental or control meat products (e.g. Vegetarians) - Refusal to follow healthy eating guidelines. - Taking medications that could affect the lipid and glycemic profiles (statins, fibrate, diuretics, corticoids, anti-inflammatory, hypoglucemic or insulin) 30 days before the beginning of the study. - Taking medications or substances for weight loss management (15 days before the beginning of the study). - Consideration to follow a weight loss diet during the duration of the study. - Pregnancy or lactation. - High intake of alcohol. - Any other exclusion criteria that the main investigator considers relevant. |
Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment
| Country | Name | City | State |
|---|---|---|---|
| Spain | IMDEA-Food | Madrid |
| Lead Sponsor | Collaborator |
|---|---|
| IMDEA Food |
Spain,
Nagao T, Watanabe H, Goto N, Onizawa K, Taguchi H, Matsuo N, Yasukawa T, Tsushima R, Shimasaki H, Itakura H. Dietary diacylglycerol suppresses accumulation of body fat compared to triacylglycerol in men in a double-blind controlled trial. J Nutr. 2000 Apr;130(4):792-7. — View Citation
Pearson AM. (1997). Principles and applications in production of reduced and low fat products. In: Production and processing of healthy meat, poultry and fish products. Advances in meat research. Vol 11. Pearson AM, Dutson TR (Eds). Blackie Academic & Professional
Rudkowska I, Roynette CE, Demonty I, Vanstone CA, Jew S, Jones PJ. Diacylglycerol: efficacy and mechanism of action of an anti-obesity agent. Obes Res. 2005 Nov;13(11):1864-76. Review. — View Citation
Saito S, Yamaguchi T, Shoji K, Hibi M, Sugita T, Takase H. Effect of low concentration of diacylglycerol on mildly postprandial hypertriglyceridemia. Atherosclerosis. 2010 Dec;213(2):539-44. doi: 10.1016/j.atherosclerosis.2010.07.062. Epub 2010 Aug 19. — View Citation
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Changes in waist circumference | The waist circumference (WC) was measured using a Seca 201 inelastic tape (Quirumed, Valencia, Spain). | Before and after 8 weeks | No |
| Secondary | Changes in lipid profile | To evaluate lipid improvements the following measurements will be taking into account: Triglycerides Total Cholesterol Low Density Lipoprotein Very Low Density Lipoprotein High Density Lipoprotein Apolipoprotein B100 Apolipoprotein E Free fatty acids |
Before and after 8 weeks | No |
| Secondary | Changes in fat depots | To evaluate changes in fat depots leptin levels will be measured | Before and after 8 weeks | No |
| Secondary | Changes in blood clotting and endothelial function | To evaluate changes in blood clotting and endothelial function will be taken into account: PAI I Fibrinogen |
Before and after 8 weeks | No |
| Secondary | Product safety | To con trol the safety of the products the following variables will be measured: Urea Creatinine GOT GPT |
Before and after 8 weeks | Yes |
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