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Nutritional Intervention clinical trials

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NCT ID: NCT03886597 Completed - Healthy Clinical Trials

Nutritional Intervention With Table Olives in Healthy Volunteers

BIOLIVA
Start date: March 25, 2019
Phase: Phase 1/Phase 2
Study type: Interventional

Olives and olive oil are typical components of the Mediterranean diet being part of its cultural and gastronomic heritage. Since ancient times, olives have been used either for both, oil extraction or whole fruit consumption as table olives. Olive oil stands out from both the nutritional and the health point of view. However, the effect of table olives consumption remains almost unknown. The beneficial properties of olive oil have been initially ascribed to the high concentration of oleic acid. Nowadays, these positive effects have been attributed also to minor compounds such as polyphenols or pentacyclic triterpenes. Table olives contain a higher amount of both polyphenols and pentacyclic triterpenes than their oil, with the same healthy fatty acid profile. Therefore, the present intervention aims at investigating the pharmacokinetic of polyphenols and pentacyclic triterpenes after a single olive intake as well as the assessment of the effect of the consumption of olives during 30 days on the overall health status playing particular attention to the anti-inflammatory, antioxidant and cardiovascular biomarkers.

NCT ID: NCT03672513 Completed - Menopause Clinical Trials

Short-term Supplementation, Bone Turnover and Antioxidant Status in Menopause

Start date: September 8, 2016
Phase: N/A
Study type: Interventional

This is a 8-week, double-blinded, placebo-controlled, randomized intervention trial to investigate the effects of Mg and Zn supplementation on antioxidant status and bone hormonal parameters. Participants were randomly assigned to one of three treatment groups: Placebo group (PbG: 25 women); Magnesium Group - 500 mg/day of Mg (MgG: 27 women); Zinc Group - 50 mg/day of Zn (ZnG: 26 women).

NCT ID: NCT01995110 Completed - Obesity Clinical Trials

Postprandial Blood Cell Transcriptome of Normal Weight and Obese Subjects to 3 Caloric Doses of a High-fat Meal

Start date: March 2011
Phase: N/A
Study type: Interventional

The study will quantitatively evaluate the metabolic response of normal weight and obese subjects to three high-fat meals differing in caloric dose by analysing the postprandial blood transcriptome.

NCT ID: NCT01885416 Completed - Obesity Clinical Trials

Impact of Dairy Products on Postprandial Inflammation

Start date: January 2013
Phase: N/A
Study type: Interventional

The study will quantitatively evaluate the systemic, postprandial inflammatory and metabolic response to the ingestion of three different meals in obese subjects. The administered meals will differ in the proportion of dairy products. Postprandial response will be monitored during 6 hours after meal consumption.

NCT ID: NCT01497249 Completed - Clinical trials for Nutritional Intervention

Assessing Fermentability of a Dietary Fiber

FCHO
Start date: December 1, 2011
Phase: N/A
Study type: Interventional

The objective of this study is to provide evidence for its fermentability of a dietary fiber and to collect information regarding potential health opportunities for glucose control as well as tolerability when being consumed over 7 days.

NCT ID: NCT01446068 Completed - Obesity Clinical Trials

Comparison of Postprandial Inflammation in Lean and Obese Subjects

Start date: March 2011
Phase: Phase 0
Study type: Interventional

The purpose of this study is to quantify the systemic inflammatory and metabolic response of lean subjects and obese subjects to the ingestion of three caloric doses of a high-fat meal.

NCT ID: NCT01042340 Completed - Clinical trials for Nutritional Intervention

Energy Dense Oleic Acid Formula to Geriatric Patients

Start date: December 2005
Phase: N/A
Study type: Interventional

Background and aims: Old patients seldom reach energy requirements. The effects of an oleic-acid rich formula on energy intake and appetite were studied. Methods: Recently admitted geriatric patients (n=71), likely to stay more than 1 week were randomised to receive a fat emulsion (Calogen, intervention group (IG)) or to standard care (control group (CG)). Thirty ml of the emulsion were given 3 times daily, i.e. 420 kcal, and was distributed at the regular medication rounds. Food intake and self-rated appetite were registered 2-3 days after admission and on day 8 or the day prior to discharge. Nutritional risk screening (NRS) 2002 and serum lipids and fatty acid profiles were analysed.