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Cachexia clinical trials

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NCT ID: NCT00994669 Completed - Cachexia Clinical Trials

Development of a Non-invasive Assessment of Skeletal Muscle Loss in Cancer Patients

Start date: October 2009
Phase: N/A
Study type: Observational

The long-term objective of this research is to develop a non-invasive approach for early assessment of which patients are at high risk for future development of skeletal muscle atrophy. The investigators hypothesize that the rate constant for the terminal portion of the isotope decay curve following ingestion of a single oral dose of deuterated-3-methylhistidine (D-3MH) provides an accurate measure of this increased risk and that this rate constant can be measured non-invasively from timed spot urine samples. In addition, the investigators hypothesize that ingestion of a meat-containing meal will stimulate synthesis of skeletal muscle proteins to a greater extent than a non-meat-containing meal.

NCT ID: NCT00972634 Completed - Depression Clinical Trials

Computerized Questionnaires in Assessing Symptoms, Pain, Depression, and Physical Function in Patients With Metastatic and/or Advanced Locoregional Cancer

Start date: October 2008
Phase: N/A
Study type: Observational

RATIONALE: A computer-based system for assessing symptoms may be effective for patients with metastatic or advanced cancer. PURPOSE: This clinical trial is studying how well computerized questionnaires work in assessing symptoms, pain, depression, and physical function in patients with metastatic and/or advanced local/regional cancer.

NCT ID: NCT00962234 Terminated - Lung Neoplasms Clinical Trials

Metabolism of Lipids in Advanced Cancer

Start date: October 2009
Phase: N/A
Study type: Observational

The causes of failing nutrition status in advanced cancer are not well known. The way fat is moved, stored, burned or changed into other compounds may be affected and will be followed in patients using a tracer and other blood tests. The investigators hypothesize that fat loss and wasting results from low essential fatty acid availability in the body. Changes may occur in the liver that limits distribution and availability of fat to the body as an energy source or for other essential functions.

NCT ID: NCT00933361 Completed - Advanced Cancer Clinical Trials

Individual Dose-escalated Bi-daily Subcutaneously (sc) Ghrelin in Cancer Cachexia: a Phase I/II Study

Start date: June 2009
Phase: Phase 1/Phase 2
Study type: Interventional

Cachexia, a condition of severe malnutrition, negative nitrogen balance, muscle wasting, weight loss, and anorexia, is a frequent affecting more than 80% of patients in advanced cancer disease causing a high burden on patients and their families. Nutritional, pharmacological, and behavioural interventions for cancer-related ACS and associated symptoms have, despite the importance for cancer care, limited effect on only a minority of patients. New strategies are required. Ghrelin, a 28 amino acid peptide discovered in 1999, is predominantly secreted by gastric endocrine cells and is an endogenous ligand for the growth hormone secretagogue (GHS) receptor. When administered peripherally it stimulates growth hormone secretion, food intake, triggers a positive energy balance, produces weight gain through a central mechanism involving hypothalamic neuropeptides and has anti-inflammatory effects. A recently completed trial on intravenous ghrelin in advanced cancer patients with ACS reports good tolerability and safety of single intravenous application of 2 and 8μg/kg Ghrelin. Given the facts that ACS is a major burden in patients suffering advanced cancer disease and ghrelin is a major signal for stimulating food intake, promoting positive energy balance and weight gain and may have anti-inflammatory effect it remains to be determined whether the administration of ghrelin will have a positive clinical effect on cancer anorexia/ cachexia syndrome ACS. The next logical clinical development step is a proper dose-finding study of twice daily subcutaneous administration and proof-of-concept of main outcomes.

NCT ID: NCT00919659 Completed - Pancreatic Cancer Clinical Trials

Parenteral Nutrition Support for Patients With Pancreatic Cancer

Start date: January 2002
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether the additional nutrition support is improving the nutritional status of patients suffering cancer caxechia or not.

NCT ID: NCT00899158 Completed - Pancreatic Cancer Clinical Trials

Biological Markers in Patients With Pancreatic Cancer Experiencing Weight Loss

Start date: June 2005
Phase: N/A
Study type: Observational

RATIONALE: Learning about biological markers in patients with pancreatic cancer and cachexia may help doctors predict patient outcome and may help the study of cancer in the future. PURPOSE: This laboratory study is examining biological markers in patients with pancreatic cancer experiencing weight loss.

NCT ID: NCT00895726 Completed - Clinical trials for Cancer-related Cachexia

Pilot Study of APD209 in Cancer Cachexia

Start date: March 2009
Phase: Phase 2
Study type: Interventional

Primary Objective: To assess the efficacy of APD209 in adult patients with active cachexia associated with advanced malignancy and not caused by simple starvation. Secondary Objective: To assess the safety of APD209 in patients with advanced malignancy and active cachexia.

NCT ID: NCT00878995 Completed - Clinical trials for Squamous Cell Carcinoma

Testosterone for Treating Cachexia in Patients With Squamous Cell Carcinoma

Start date: June 3, 2009
Phase: Phase 1
Study type: Interventional

RATIONALE: Testosterone may lessen weight loss and improve muscle size and strength in patients with cachexia caused by cancer. PURPOSE: This randomized phase I trial is studying whether testosterone administered during standard of care chemotherapy and/or radiation works by helping patients with squamous cell carcinoma to maintain their body weight and muscle size and strength during treatment.

NCT ID: NCT00866970 Completed - Fatigue Clinical Trials

Safety, Efficacy and Pharmacokinetics of ALD518 in Patients With Non-Small Cell Lung Cancer-related Fatigue and Cachexia

Start date: September 2008
Phase: Phase 2
Study type: Interventional

The purpose of this study is to asses the safety and efficacy of ALD518 in patients with Non-Small Cell Lung Cancer-Related Fatigue and cachexia (weight-loss).

NCT ID: NCT00852020 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Safety, Tolerance and Efficacy of an Oral Nutritional Supplement in Chronic Heart Failure and Chronic Obstructive Pulmonary Disease Patients

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

To test the compliance, tolerance, safety and to get preliminary insights into the efficacy of a new oral nutritional supplement (containing n-3 fatty acids, amino acids and antioxidants) designed to prevent or delay cachexia and anorexia in patients with chronic heart failure (CHF) or chronic obstructive pulmonary disease (COPD).