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Starvation clinical trials

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NCT ID: NCT05967858 Completed - Starvation Clinical Trials

Incidence of Refeeding Syndrome in Consecutively Admitted Patients

Start date: December 1, 2013
Phase:
Study type: Observational

The incidence and main risk-factors analyzed in consecutive in-patients in the departments og gastroenterology and ear-nose and throat diseases (cancer in radiation therapy)

NCT ID: NCT03600311 Completed - Weight Loss Clinical Trials

Resistance Exercise and Protein During Weight Loss

RIDE
Start date: August 31, 2018
Phase: N/A
Study type: Interventional

The purpose of this study is to determine if post-exercise protein supplementation can rescue the anabolic response of muscle and bone to resistance exercise during caloric restriction.

NCT ID: NCT03573063 Completed - PCOS Disease Clinical Trials

Studying the Starvation Effect on Androgen Metabolism in 20 Healthy Young Women and Comparison to Women With PCOS.

SEA
Start date: October 26, 2018
Phase: N/A
Study type: Interventional

In this study, the investigators wanted to investigate the energy homeostasis and the steroid metabolism of 20 healthy, young and normal weight women aged between 16-35 years before and after a 48 hours fasting period. The following substrates and hormone concentrations representing the carbohydrate, fat and protein metabolism will be measured from plasma or urine before and after fasting: glucose, insulin, lactate, alpha-synucleine, free fatty acids, beta-hydroxybutyrate (ketone bodies), carnitine (surrogate for acetyl-CoA) and alanine (amino acids). In addition, the investigators will measure 67 steroid metabolites by GC/MS and Biokrates AbsolutIDQ Steroid Assay in all collected urines and blood samples. In the analysis of the data, the investigators will focus on correlations between biochemical parameters of the energy metabolism and parameters of the steroid metabolism, specifically the androgens. In addition, the steroid profiles obtained from healthy young women before and after fasting will be compared to steroid profiles of PCOS women in search for specific differences.

NCT ID: NCT02945410 Completed - Weight Loss Clinical Trials

Effect of Caloric Restriction and Protein Intake on Metabolism and Anabolic Sensitivity

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

The purpose of this study is to determine if an increased protein intake can attenuate the suppression of metabolic and anabolic hormones during caloric restriction

NCT ID: NCT00943020 Completed - Starvation Clinical Trials

Effects of Glutamine on Gastric Emptying

Start date: July 2009
Phase: Phase 4
Study type: Interventional

Surgical patients are usually starved for 8 hours before operation in order to ensure the stomach is empty and thus reduce the chances of vomiting during the anaesthetic. Recent studies have shown that this period of starvation is harmful as it 'weakens' the body before operation. To avoid the harmful effects of starvation, patients are now given carbohydrate (sugar-containing) drinks 2 to 4 hours before surgery. These drinks have been shown to make patients feel better, reduce sickness after the anaesthetic/surgery and result in a quicker recovery from operation. The optimum time of giving these drinks to patients before operation is unknown. Previous studies have shown that the drinks empty from the stomach within 2 - 4 hours depending on their ingredients. The investigators would like to study the effects of adding protein and fat to these drinks on how quickly the drinks empty from the stomach. This study will investigate the hormone responses of the body following intake of 3 different drinks in order to determine the mechanisms that underlie the control of stomach emptying. This information will also allow us to improve the design of these drinks and this could help patients who undergo surgery who receive them.

NCT ID: NCT00909701 Completed - Starvation Clinical Trials

Metabolic Response Following Intake of 2 Metabolic Preconditioning Drinks

Start date: May 2009
Phase: N/A
Study type: Interventional

Surgical patients are usually starved for 8 to 12 hours before operation in order to reduce the chances of vomiting and other complications during the anaesthetic. Recent studies have suggested that this period of starvation might be harmful as it 'weakens' or 'stresses' the body before the operation. To avoid these harmful effects of starvation, patients are now given carbohydrate drinks (sugar-containing drinks that provide energy for the body) up to 2 hours before the operation. These drinks have been shown to make patients feel better, reduce sickness after the anesthetic/surgery and result in quicker recovery from operation. But the ways in which the sugar drinks have these beneficial effects on the body are unknown. The optimum time of giving these drinks to patients before operation is also unknown. This study will investigate the hormone responses of the body, following intake of 2 different carbohydrate drinks, in order to determine the optimum time of intake of these drinks in order to obtain the maximum benefits for the body.

NCT ID: NCT00574431 Completed - Critical Illness Clinical Trials

ICU Nutrition Study Bern

Start date: February 2008
Phase: Phase 4
Study type: Interventional

Nutritional treatment has become an essential component of the management of critically ill, due to better knowledge about positive impact of nutritional support. Malnutrition among ICU patients is associated with increased morbidity, mortality, length of stay (LOS) and therefore higher costs.Several studies however suggest, that early implementation of nutritional support is associated with improved clinical outcome, shorter LOS, and decreased infection rates. One of the objectives of this study is to determine if an nutrition protocol can improve the delivery of enteral tube feeding in the ICU.

NCT ID: NCT00574119 Completed - Heart Failure Clinical Trials

Effect of Aldosterone on Energy Starvation in Heart Failure

Start date: December 2007
Phase: Phase 4
Study type: Interventional

We plan to study the concept of "energy starvation" in heart failure by evaluation of patients with nonischemic dilated cardiomyopathy (NIDCM) (heart failure with reduced heart pump function due to causes other than heart attack). We will use a combination of positron emission tomography and magnetic resonance imaging to study metabolism, anatomy, function, blood flow and efficiency, before and after 6 months' treatment with the drug spironolactone which blocks the deleterious effects of the hormone aldosterone on the myocardium (heart muscle).

NCT ID: NCT00260286 Completed - Infertility Clinical Trials

Effects of Gynecological Age on LH Sensitivity to Energy Availability

Start date: August 2001
Phase: N/A
Study type: Interventional

The purpose of this experiment is to investigate whether the dependence of luteinizing hormone pulsatility on energy availability declines during adolescence.