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Nutritional Support clinical trials

View clinical trials related to Nutritional Support.

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NCT ID: NCT06397430 Completed - Postoperative Clinical Trials

Nutritional Support for Patients Operated for Malignant Tumors in HPD Zone

Start date: December 1, 2017
Phase: N/A
Study type: Interventional

A comprehensive comparative analysis of the effectiveness of isolated enteral, isolated parenteral and mixed type of nutritional support in the early postoperative period in patients after operations performed on the malignant neoplasms of hepatico-pancreatico-duodenal zone.

NCT ID: NCT03634943 Completed - Critical Illness Clinical Trials

Evaluation of Nutritional Practices in the Critical Care

ENPIC
Start date: April 23, 2018
Phase:
Study type: Observational

Background: The adequacy of the artificial Nutritional Support (NS) in the critical care patient has implications in morbidity and prognosis. Clinical practice guidelines (CPG) are an important tool for healthcare professionals in their daily practice and a method of consultation for the correct treatment of patients. Also, the evidence remains low and there are important controversies regarding the NS in the critical care patient. Hypothesis: The NS generates great controversy in the professionals involved in the care of critical care patients due to the contradictory results in literature. Despite this, the CPG should serve to standardize the treatment of patients and provide a better adherence to current knowledge in this setting. The importance of NS is underestimated and there is a need to perform proper evaluation of the impact of nutrition. Objectives: To evaluate and analyze NS practices in critically ill patients in different ICUs and assess the adherence to CPGs. To evaluate the relationship of nutrition and outcomes in the ICU. Methodology: Prospective multicenter observational study. Collection of variables from different participating ICUs and the characteristics of the NS of the different admitted patients. Monitoring of nutritional practices and complications. Evaluation of outcomes (e.g. mortality, ICU complications, etc.) with NS. Expected results: Better understanding of the NS and its impact on morbidity and mortality; development of strategies to reduce low adherence to CPGs, improving the quality of care associated with this field in critical care patients; obtain clinical information that will serve as a basis for conducting intervention studies.

NCT ID: NCT03400046 Completed - Muscle Loss Clinical Trials

The Correlation Between Nutrients and Muscle Mass

Start date: September 1, 2013
Phase: N/A
Study type: Observational

Patients who are suffer from CIF often develop muscle wasting because of hypercatabolism.The relationship between different nutrition support formulas and lean body mass is still unclear. The purpose of this study is to investigate the relationship between nutrition support and muscle mass and attempt to find the nutrients which will benefit lean body mass in patients with CIF.

NCT ID: NCT03115931 Completed - General Surgery Clinical Trials

The Effect of Preoperative Nutritional Assessment and Nutritional Support on Clinical Outcomes

PNAS
Start date: April 14, 2017
Phase:
Study type: Observational

It is a study to evaluate the relationship between preoperative nutritional assessment and clinical outcomes and to explore the effect of preoperative nutritional support on clinical outcomes in patients after abdominal operation.

NCT ID: NCT02580214 Completed - Perioperative Care Clinical Trials

Immunonutrition in Total Hip Arthroplasty

Immunehip
Start date: May 2013
Phase: Phase 2/Phase 3
Study type: Interventional

The aim of this pilot study was to investigate whether the use of a multimodal protocol of preoperative care plus preoperative immune nutrition would decrease the length of stay and acute phase inflammation in patients submitted to total hip arthroplasty (THA). The study was designed to be randomized and controlled, but not double blind. The patients were randomized to receive either preoperative care based on evidence plus immune nutrition for 5 days prior to surgery (Acerto group) or traditional preoperative care (control group). Main endpoints were length of stay and acute-phase postoperative response