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Fatigue clinical trials

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NCT ID: NCT00790296 Terminated - Clinical trials for Cancer-related Fatigue

Evaluation of Synthetic Thyrotropin Releasing Hormone (TRH) as a Treatment for Cancer-related Fatigue

Start date: December 2006
Phase: Phase 2
Study type: Interventional

The primary objective of the study is to evaluate thyrotropin releasing hormone (TRH) as a treatment for cancer-related fatigue. The central hypothesis of this pilot study is that TRH is more efficacious than placebo in alleviating cancer-related fatigue in patients with breast or prostate cancer.

NCT ID: NCT00789620 Completed - Pain Clinical Trials

Effects of Intravenous Lidocaine on Transperitoneal Laparoscopic Urological Surgery

Start date: November 2008
Phase: Phase 3
Study type: Interventional

Effective perioperative analgesia is the key to postoperative rehabilitation. An intriguing body of evidence suggests that short-term administration of intravenous lidocaine may produce pain relief that far exceeds both the duration of infusion and the half-life of the drug. When pain relief is provided, concomitant anal-gesic medication can be reduced, side effects from pain relieving medication minimized with a potential for a more rapid postoperative recovery and less complications. IV application of lidocaine should de-crease the duration of bowel dysfunction. We hypothesise that i.v. application of lidocaine in a standard antiarrythmic dose can significantly improve acute rehabilitation after laparoscopic urological surgery and so shorten the hospital stay (primary outcome). We expect that the intraoperative inflammatory response can significantly be reduced.

NCT ID: NCT00775645 Completed - Breast Cancer Clinical Trials

S0715: Acetyl-L-Carnitine in Preventing Neuropathy in Women With Stage I, Stage II, or Stage IIIA Breast Cancer Undergoing Chemotherapy

Start date: September 2009
Phase: Phase 3
Study type: Interventional

RATIONALE: Acetyl-L-carnitine may prevent or lessen neuropathy caused by chemotherapy. It is not yet known whether acetyl-L-carnitine is more effective than a placebo in preventing neuropathy caused by chemotherapy. PURPOSE: This randomized phase III trial is studying acetyl-L-carnitine to see how well it works compared with a placebo in preventing neuropathy in women with stage I, stage II, or stage III breast cancer undergoing chemotherapy.

NCT ID: NCT00772226 Completed - Pain Clinical Trials

The Use of Music as Pain Therapy in Patients Undergoing Laparoscopic Cholecystectomy in a Day Care Unit

Start date: September 2008
Phase: Phase 3
Study type: Interventional

The study is undertaken to investigate whether relaxing music therapy before, during and after laparoscopic cholecystectomy has any effect on pain, PONV or fatigue and level of stress as measured by Cortisol and C reactive protein. Patients will be scored according to those endpoints 1 and 3 hours after surgery and on day 1 and 7 post-OP.

NCT ID: NCT00769301 Completed - Depression Clinical Trials

Symptom Clusters in Cancer Patients and Their Caregivers- a Longitudinal Study

Start date: November 2008
Phase:
Study type: Observational

The complexity of cancer patients' symptoms and health problems constitutes considerable distress and burden for patients and their family caregivers. To help them manage the illness effectively, there is a need to better understand the complexity of symptoms and symptom clusters in patients and caregivers. Therefore, the purpose of this research is to explore a set of important fundamental research questions to advance the scientific knowledge of cancer patients' and caregivers' symptoms, symptom clusters and health-related quality of life. The investigators will follow 500 cancer patients and their caregivers with repeated measures over 6 months to assess their symptoms, symptom clusters, and quality of life over time. Caregiver burden will also be examined in the caregivers.

NCT ID: NCT00764231 Completed - Quality of Life Clinical Trials

A Study of a Home-based Exercise Intervention for Patients With Acute Myeloid Leukaemia (AML)

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

Fatigue is the most common and disabling symptom in acute myeloid leukaemia (AML). Studies in other cancer patients with fatigue have shown that exercise improves both fatigue and quality of life (QOL), but there are no such studies in AML. The investigators want to conduct a pilot study of a home-based exercise program to see if this type of exercise program is feasible for AML patients, reduces fatigue, and improves QOL. What the investigators learn from this study will be essential to designing a larger, definitive randomized trial of exercise in patients with AML.

NCT ID: NCT00758407 Completed - Clinical trials for Cancer-related Fatigue

Methylphenidate Treatment of Cancer-Related Fatigue

EMF
Start date: August 2006
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this randomized controlled clinical trial is to investigate the efficacy and safety of methylphenidate in patients with fatigue caused by cancer.

NCT ID: NCT00755313 Completed - Breast Cancer Clinical Trials

Effects of Chemotherapy on the Brain in Women With Newly Diagnosed Early-Stage Breast Cancer

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

RATIONALE: Gathering information over time from laboratory tests, imaging scans, and assessment tests may help doctors learn more about the side effects of chemotherapy and plan the best treatment. PURPOSE: This clinical trial is studying the effects of chemotherapy on the brain in women with newly diagnosed early-stage breast cancer.

NCT ID: NCT00737204 Completed - HIV Infections Clinical Trials

Effectiveness of Armodafinil for Treating Fatigue in Adults With HIV/AIDS

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

This study will determine whether armodafinil (Nuvigil), an FDA approved medication, is effective in reducing fatigue in adults with HIV/AIDS.

NCT ID: NCT00731991 Completed - Fatigue Clinical Trials

Art and Surface Electromyography (EMG)

Start date: August 2008
Phase: Phase 1/Phase 2
Study type: Interventional

The general purpose of this research project is to use surface electromyography to compare the effect of Active Release Technique versus Proprioceptive Neuromuscular Facilitation on the electrical activity of the upper trapezius muscle at rest and during contraction.