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NCT ID: NCT01620411 Withdrawn - Pain Clinical Trials

War Wounded, a Comparison of Two Pain Management Approaches

Start date: June 2012
Phase: N/A
Study type: Interventional

This study aims to investigate the relative effectiveness of two different pain management plans for injuries sustained while active duty in the military. One arm of the study has subjects undergo standard comprehensive medical management, while the other adds the placement of a spinal cord stimulator, a common procedure for the alleviation of pain.

NCT ID: NCT01620229 Withdrawn - Clinical trials for Hematopoietic/Lymphoid Cancer

Brentuximab Vedotin After Donor Stem Cell Transplant in Treating Patients With Hematologic Malignancies

Start date: June 2013
Phase: Phase 1/Phase 2
Study type: Interventional

This phase I/II trial studies the side effects and best way to give brentuximab vedotin and to see how well it works after donor stem cell transplant in treating patients with hematologic malignancies. Monoclonal antibodies, such as brentuximab vedotin, can block cancer growth in different ways. Some block the ability of cancer to grow and spread. Others find cancer cells and help kill them or carry cancer-killing substances to them. Monoclonal antibodies may kill cancer cells that are left after donor stem cell transplant.

NCT ID: NCT01619566 Withdrawn - Fibromyalgia Clinical Trials

Cymbalta for Fibromyalgia Pain - Predictive Value of Small Fiber Changed

Start date: June 2012
Phase: Phase 4
Study type: Interventional

Subjects with Fibromyalgia who respond to Duloxetine have specific nerve fiber characteristics. This can be used to predict which future patients will respond to Duloxetine.

NCT ID: NCT01619449 Withdrawn - Clinical trials for Chronic Kidney Disease

Continuous Renal Replacement Therapy in the Setting of Orthotopic Liver Transplant

Start date: April 2012
Phase: N/A
Study type: Interventional

To evaluate the efficacy of continuous renal replacement therapy (CRRT) during orthotopic liver transplantation (OLT) in clearing excess solutes and improving acid-base parameters. The investigators hypothesize that the use of intra-operative CRRT in OLT recipients is associated with increased solute removal and improved acid-base statues when compared to controls who do not receive CRRT

NCT ID: NCT01618253 Withdrawn - Clinical trials for Hepatocellular Carcinoma

Radiation Therapy With Sorafenib for TACE-Resistant Hepatocellular Carcinoma

Start date: June 2012
Phase: Phase 1
Study type: Interventional

To determine the maximum tolerated radiation dose with concurrent sorafenib for unresectable hepatocellular carcinoma that has not responded to transarterial chemoembolization.

NCT ID: NCT01617798 Withdrawn - Respiratory Failure Clinical Trials

Stop Hypernatremia, Use Metolazone, for Aggressive, Controlled, Effective Diuresis

SHUM
Start date: June 2012
Phase: N/A
Study type: Interventional

Patients who are on mechanical ventilation in an intensive care unit often require diursis as part of their pre-extubation regimen. The drug of choice for diuresis has traditionally been furosemide. However, this drug cause hypernatremia (a rise in serum sodium) in a significant proportion of patients. Hypernatremia is traditionally treated by providing free water supplementation to the patient. This strategy creates a vicious and unproductive cycle of giving free water, and then diuresing it off. We propose a strategy for breaking this cycle by using a second diuretic-- metolazone-- which has a tendency to rid the body of more sodium, thereby minimizing hypernatremia.

NCT ID: NCT01616719 Withdrawn - Clinical trials for Cervical Radiculopathy

Evaluation of DTRAX Graft in Patients With Cervical Degenerative Disc Disease

Start date: May 2012
Phase: N/A
Study type: Interventional

DTRAX Graft is used to relieve nerve pressure in the neck in order to provide relief for Cervical Degenerative Disc Disease. This study is being conducted to determine the effectiveness of the graft, and to find out whether or not it provides better results or faster healing than traditional ways of performing surgery for Cervical Degenerative Disc Disease.

NCT ID: NCT01616680 Withdrawn - Clinical trials for Graft Versus Host Disease

Brentuximab Vedotin in Treating Patients With Steroid-Resistant Acute Graft-Versus-Host Disease

Start date: September 2012
Phase: Phase 2
Study type: Interventional

The purpose of this research is to test the safety and efficacy of brentuximab vedotin in patients with acute skin graft-versus-host disease (GVHD)

NCT ID: NCT01615666 Withdrawn - Clinical trials for Mild Cognitive Impairment

A Composite MR Neuroimaging Marker for Alzheimer's Disease

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

The purpose of this study is to use a functional MRI (fMRI) index to compare the brain activity of healthy volunteers to that of people with mild cognitive impairment (MCI) and Alzheimer's disease. The ultimate goal is to develop an early diagnostic tool for Alzheimer's disease. The study hypotheses are: 1. The fMRI index will differentiate between Alzheimer's disease, non-Alzheimer's dementia, and healthy volunteers; 2. The fMRI index will distinguish participants with MCI who convert to Alzheimer's disease from those who convert to a non-Alzheimer's dementia and those who remain stable; 3. MCI participants with a lower fMRI index at baseline who convert will progress to Alzheimer's sooner than those with a higher fMRI index, and MCI participants with a faster rate of fMRI index decline who convert will have an earlier onset of Alzheimer's disease.

NCT ID: NCT01615055 Withdrawn - Clinical trials for Cognitive Dysfunction

Fluoxetine Prevention Trial

Start date: June 2018
Phase: Early Phase 1
Study type: Interventional

Many cancer survivors are experiencing problems with memory and other cognitive abilities following cancer treatment. Little is known concerning the contributions of potentially preventive therapies on cognitive function, but animal studies have pointed to the potential value of the medication fluoxetine in this context. We aim to determine whether six months of fluoxetine therapy can preserve brain function in patients who have undergone chemotherapy, and examine potential biological mechanisms for its protective effects in humans. If use of fluoxetine in cancer patients can be validated in this manner, it will represent the first drug demonstrated to prevent cerebral dysfunction associated with exposure to chemotherapy. Moreover, as this involves an agent that is already FDA-cleared for other indications, widely commercially available throughout the U.S. and other parts of the world, and relatively inexpensive since it is obtainable in generic formulations, it would represent a pharmacologic approach that is amenable to rapid translation to the clinical setting.