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Cachexia clinical trials

View clinical trials related to Cachexia.

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NCT ID: NCT03207724 Completed - Pancreatic Cancer Clinical Trials

Study of Onivyde and 5-FU in Combination With Xilonix for Pancreatic Cancer With Cachexia

OnFX
Start date: October 16, 2017
Phase: Phase 1
Study type: Interventional

This study is being conducted to examine the safety of the investigational drug, Xilonix(™), in addition to standard doses of Onivyde® (nanoliposomal irinotecan) and 5- fluorouracil (5FU)/folinic acid (leucovorin) for pancreatic cancer patients with cachexia. Cachexia is a syndrome that includes involuntary weight loss and physical deterioration that can contribute to poor outcomes of cancer treatment. In other studies, Xilonix has increased lean body mass in advanced cancer patients. This increase could lead to improved weight maintenance and quality of life.

NCT ID: NCT03162042 Completed - Clinical trials for Head and Neck Cancer

Role of Myostatin, Activin A and Follistatin Cachexia of ENT Cancers

MYOCACH
Start date: November 2, 2015
Phase: N/A
Study type: Observational

The main objective of our study was to determine the modifications of blood myostatin and activin A concentrations associated with head and neck cancers. Secondary objectives consisted in studying their influence on the occurrence of cachexia, bringing the proof of a tumoral secretion of these factors, and then determining the effect of tumor removal.

NCT ID: NCT03144128 Completed - Clinical trials for Vitamin D Deficiency

Vitamin D for Muscle Metabolic Function in Cancer Cachexia

Start date: May 23, 2018
Phase: N/A
Study type: Interventional

The proposed study is aimed at examining mitochondrial function as a potential target of action of vitamin D on muscle metabolism, size, and strength in preventing the progression of cachexia. This is the first clinical trial designed to understand the effects of vitamin D on muscle metabolic dynamics driving dysfunction in cachectic muscle. Our preliminary data suggest that vitamin D promotes lipid partitioning and muscle metabolic function, which the investigators hypothesize, will mitigate cachexia via improved muscle health and quality that translates into reduced fatigue, and improved patient resilience to multimodal cancer therapy.

NCT ID: NCT03135717 Completed - Clinical trials for Chronic Kidney Hospitalized

Wasting in Chronic Kidney Disease

PEW
Start date: December 2011
Phase: N/A
Study type: Observational

Protein energy wasting is an independent factor associated with morbi-mortality in chronic kidney disease. Wasting is particularly common in chronic diseases of organs such as kidney disease with a major impact at the stage of dialysis. It covers 20 to 70% of patients diagnosed with chronic kidney disease according to the degree of evolution of the disease and the diagnostic method. Mechanisms of PEW are based mainly on anorexia and metabolic abnormalities caused by kidney disease. Nutritional treatment differs depending on the stage of the kidney disease acute or chronic treated whether or not by dialysis. Nutritional monitoring should be regular, individualized and collaborative to detect a risk of PEW or treat installed PEW. Refeeding techniques should allow all the nutritional needs. Their indications depend on the clinic, biochemical assessment and nutrient intake.

NCT ID: NCT03042442 Completed - Pain Clinical Trials

Relation Between Cachexia, Diabetes and periNeural Invasion in PANcreatic Cancer- Biomarkers Substudy

CDNPAN
Start date: January 1, 2017
Phase:
Study type: Observational

The purpose of this study is to determine the interrelationship between cachexia, neural invasion and diabetes in patients with pancreatic cancer. Thus the investigators propose to identify the protein expression levels of Activin and Midkine in plasma of patients with different stages of pancreatic adenocarcinoma compared with healthy patients and to evaluate the possible correlation with diabetes, tumor size and tumor stage.

NCT ID: NCT03026985 Completed - Critical Illness Clinical Trials

Acute Skeletal Muscle Wasting and Relation to Physical Function in Patients Requiring ECMO

Start date: January 25, 2017
Phase: N/A
Study type: Observational

The purpose of this study is to describe the changes in quadriceps muscle size and quality over the first 10 days on extracorporeal membrane oxygenation (ECMO) using ultrasound imaging. This study will also examine the relationship between those changes and muscle strength and level of physical function at day 10 and day 20 after ECMO commencement.

NCT ID: NCT03012139 Completed - Metastatic Cancer Clinical Trials

Cancer-Associated Muscle Atrophy and Weakness: An Investigation of Etiology

Start date: January 2017
Phase:
Study type: Observational

This study is designed to gain a better understanding of the mechanisms leading to muscle wasting and metabolic abnormalities in skeletal muscle of cancer patients.

NCT ID: NCT02983500 Completed - Clinical trials for Metastatic Pancreatic Cancer

Patient Reported Outcomes Registry in Patient With Cancer Cachexia

PROXie
Start date: August 28, 2016
Phase:
Study type: Observational

Evaluation of patient reported outcomes (PRO) with tumor cachexia in a real life setting.

NCT ID: NCT02968979 Completed - Clinical trials for Non-small Cell Lung Cancer

Non-interventional Study to Assess the Frequency of Cachexia in Patients With Non-small Cell Lung Cancer.

CacheMire
Start date: July 2016
Phase:
Study type: Observational

The purpose of this study is to assess the frequency of cachexia and the management of cachexia and associated symptoms in a patient population with non-small cell lung cancer (NSCLC).

NCT ID: NCT02962089 Completed - Undernutrition Clinical Trials

Microbiota and Protein-energy Wasting (MIDIWA)

MIDIWA
Start date: August 2016
Phase: N/A
Study type: Interventional

Oral supplementation with branched chain amino acids (BCAA) increases the levels of circulating BCAA, stimulates BCAA uptake in muscles, and decreases amino acid release from muscle, eventually promoting muscle anabolism. However, uptake of oral BCAA by muscle is not complete, pointing out that non-muscular tissues, as the splanchnic bed and gut microbiota, may play a role in BCAA metabolism. This protocol aims at studying the impact of protein-energy wasting (PEW) and of refeeding with branched chain amino acids (BCAA), on gut barrier including gut microbiota, in chronic hemodialysis (HD) patients. The investigators speculate that: 1. HD patients with PEW have altered composition and function of gut microbiota, increased permeability of epithelial gut barrier, increased systemic inflammation but decreased fecal immunoglobulin A (IgA), and a dysbalance of plasma appetite mediators in favor of anorexigenic mediators, compared to HD patients without PEW, non dialyzed patients with chronic kidney disease and well-nourished non obese subjects, 2. BCAA supplementation of HD patients with PEW reverses these changes, thereby improving nutritional state, physical function, quality of life and resistance to infections.