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Fatigue clinical trials

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NCT ID: NCT01156922 Terminated - Clinical trials for Chronic Fatigue Syndrome

B-cell Depletion Using the Monoclonal Anti-CD20 Antibody Rituximab in Very Severe Chronic Fatigue Syndrome

Start date: June 2010
Phase: Phase 2
Study type: Interventional

Based on pilot patient observations, and experience from the prior study KTS-1-2008, the investigators anticipate that severely affected chronic fatigue syndrome patients may benefit from B-cell depletion therapy using Rituximab induction with maintenance treatment. The hypothesis is that at least a subset of chronic fatigue syndrome (CFS) patients have an activated immune system involving B-lymphocytes, and that prolonged B-cell depletion may alleviate symptoms. An approved amendment (April 15th 2011): the study will be extended with up to 5 patients. For up to 5 patients in the study, standard plasma exchange may be performed 2-3 weeks prior to start of B-lymphocyte depletion using Rituximab (as in the protocol). Approved amendment (December 2011): for patients with gradual improvement in CFS/ME symptoms after 12 months follow-up, but not having reached a clear response, up to 6 additional Rituximab infusions (500 mg/m2, max 1000 mg) may be given during the following 12 months period.

NCT ID: NCT01156909 Completed - Clinical trials for Chronic Fatigue Syndrome

B-cell Depletion Using the Monoclonal Anti-CD20 Antibody Rituximab in Chronic Fatigue Syndrome

Start date: October 2010
Phase: Phase 2
Study type: Interventional

Based on pilot patient observations, and experience from the prior study KTS-1-2008, the investigators anticipate that chronic fatigue syndrome patients may benefit from B-cell depletion therapy using Rituximab induction with maintenance treatment. The hypothesis is that at least a subset of CFS patients have an activated immune system involving B-lymphocytes, and that prolonged B-cell depletion may alleviate symptoms.

NCT ID: NCT01149525 Completed - Multiple Sclerosis Clinical Trials

Efficacy of L-carnitine Versus Placebo in the Treatment of Fatigue in Multiple Sclerosis

FACTSEP
Start date: June 2010
Phase: Phase 3
Study type: Interventional

The objective of this study is to evaluate the efficacy of L-carnitine versus placebo in the treatment of fatigue in multiple sclerosis patients. This study will randomize 60 patients in a cross-over design. This study is sponsored by academic French health institutions.

NCT ID: NCT01143467 Completed - Cancer Clinical Trials

Relationship Between Mitochondrial Dysfunction and Fatique in Cancer Patients Following External Beam Radiation Therapy

Start date: May 24, 2010
Phase: N/A
Study type: Observational

Background: - Fatigue is a very common early and late side effect of cancer treatment, including radiation therapy. The cause of fatigue is poorly understood, making it hard to diagnose and treat. More research is necessary to understand why patients receiving cancer treatment experience fatigue. Changes in mitochondria, parts of body cells that help provide energy to the cell, may contribute to fatigue. Researchers are interested in looking at blood chemicals and mitochondrial genes of cancer patients to study those associated with fatigue. Objectives: - To study the relationship between fatigue and the effects of cancer treatment. Eligibility: - Men at least 18 years of age who have been diagnosed with localized prostate cancer and are scheduled to receive external beam radiation therapy. - Participants on study 09-NR-0088, Molecular-Genetic Correlates of Fatigue in Cancer Patients Receiving External Beam Radiation Therapy, are also eligible. Design: - This study requires three outpatient visits to the NIH Clinical Center. - Participants will be seen before they start radiation treatment, at the middle of treatment, and at the end of treatment. Each visit will take less than 30 minutes to complete. - Participants will complete questionnaires that ask about fatigue and depression. - Participants will provide blood samples for research testing and potential HIV testing. - No treatment will be provided as part of this protocol.

NCT ID: NCT01125982 Completed - Fatigue Clinical Trials

Postoperative Fatigue and Nausea Related to Choice of Anaesthetic Regimens

Start date: June 2010
Phase: Phase 4
Study type: Interventional

The purpose of this study is to establish validated outcome measures for Postoperative Fatigue and Postoperative nausea, and to compare clinical impact of postanaesthetic symptoms during first week after Propofol or Desflurane based anaesthesia.

NCT ID: NCT01117896 Completed - Clinical trials for Rescuer Fatigue During CPR

CPR Rescuer Fatigue on Chest Compression Effectiveness

Start date: May 2007
Phase: N/A
Study type: Interventional

This prospective, randomized experimental trial to determine whether the quality of healthcare provider/rescuer chest compressions (CC) deteriorates at the same rate in pediatric models as compared to adult models. To determine the relationship between physiologic/metabolic markers of work in rescuers and chest compression deterioration, and to determine the effect of stepstool use on the quality of chest compressions and metabolic demand. To determine whether the quality of chest compressions deteriorates at the same rate in participants using a stepstool compared to those not using a stepstool.

NCT ID: NCT01113905 Terminated - Breast Cancer Clinical Trials

Role of Beta-Endorphin in Cancer Therapy Fatigue

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

The investigators aim to test whether beta-endorphin, a substance our bodies make in response to painful and stressful stimuli, plays a causative role in radiation-induced fatigue that cancer patients receiving radiation therapy commonly experience. If this is so, the investigators' hope is to direct efforts at treating radiation-induced fatigue using agents that block the action of beta-endorphin with the aim of improving quality of life for patients undergoing radiation therapy

NCT ID: NCT01108549 Completed - Fibromyalgia Clinical Trials

Treatment of Chronic Fatigue Syndrome and Fibromyalgia With D-ribose- a Multicenter Study

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

To determine whether adding Ribose 5 grams 3 x day would improve quality of life, energy, sleep and cognitive function and decrease pain in patients with CFS and/or fibromyalgia (CFS/FMS).

NCT ID: NCT01106820 Completed - Breast Cancer Clinical Trials

Progressive Resistance Training Versus Relaxation for Breast Cancer Patients During Chemotherapy: Biological Mechanisms and Effects on Fatigue and Quality of Life

BEATE
Start date: April 2010
Phase: N/A
Study type: Interventional

The purpose of this randomized intervention study is to investigate the effects and biological mechanisms of a supervised 12-week progressive resistance training on fatigue and quality of life in breast cancer patients during chemotherapy. To determine the effect of the exercise itself beyond potential psychosocial effects due to attention by trainers or the group support, patients in the control group have a comparable training schedule (i.e. 60 min, twice a week, for 12 weeks) but with relaxation training (Jacobsen method).

NCT ID: NCT01100632 Suspended - Clinical trials for Reduction of Stress and Fatigue

Effectiveness Evaluation of Panax Ginseng, Vitamins and Minerals in Improvement of Stress and Fatigue

Start date: September 2010
Phase: Phase 3
Study type: Interventional

We hope that with the drug, patients obtain reduced levels of stress and fatigue, according to the scales that we use in the study. Hopefully the results of the treated group are significantly higher than the control group (placebo).