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NCT ID: NCT02757157 Terminated - Clinical trials for Pulmonary Disease, Chronic Obstructive

Comparison of Walking in Water and on Land in People With Chronic Obstructive Pulmonary Disease (COPD)

Start date: October 2016
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the metabolic load during a single session of moderate intensity walking in water compared to walking on land (over-ground) in people with chronic obstructive pulmonary disease (COPD) who are normal weight and obese, compared with peak exercise metabolic response. The hypothesis is that the metabolic load of walking at a moderate intensity in water will be greater than walking on land.

NCT ID: NCT02755948 Terminated - Influenza, Human Clinical Trials

A Study of Protective Immunity Against RSV and Influenza in Experimental Human Challenge of Volunteers

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

Respiratory viruses including influenza and respiratory syncytial virus (RSV) are among the most important causes of severe disease globally, infecting everyone repeatedly throughout life. Understanding of how to prevent infection is incomplete but boosting immunity with vaccines remains the best strategy. T cells have been shown in animals to be essential for clearing respiratory viral infection and are likely to be helpful if stimulated by vaccines. However, where these cells originate from and how they develop in the human lung are still unclear. The investigators will inoculate volunteers with influenza or RSV to examine the relationship between T cells in their blood and lungs and the outcome of infection. By tracking these specialised cells, the investigators aim to develop a better understanding of how they are generated in order to harness them with future vaccines.

NCT ID: NCT02755155 Terminated - Shock Clinical Trials

Optimization of Therapeutic Human Serum Albumin Infusion in Selected Critically Ill Patients

AlbAlsace
Start date: September 2016
Phase: Phase 4
Study type: Interventional

Primary purpose : mortality at Day 28 Secondary purposes : - Daily SOFA (Sequential Organ Failure Assessment) score lessening within Intensive Care Unit (ICU) - Duration of increasing doses of norepinephrine infusion to maintain target mean arterial pressure - Number of care-related infections within ICU

NCT ID: NCT02754466 Terminated - Dental Caries Clinical Trials

Oral Health and Its Relation to Development and Well-being of Schoolchildren Before and After Restorative Treatments

Start date: May 2, 2017
Phase: N/A
Study type: Interventional

The present study aims evaluate the oral health conditions of schoolchildren and its relation to growth, development and well-being. Also, it seeks to evaluate different restorative interventions performed at school premises in primary teeth and its impact on the quality of life.

NCT ID: NCT02749708 Terminated - Clinical trials for Acute Myeloid Leukemia (AML)

Study of IRX5183 in Relapsed and Refractory Acute Myeloid Leukemia and High Risk Myelodysplastic Syndrome

Start date: January 30, 2017
Phase: Phase 1
Study type: Interventional

The purpose of this study is to evaluate the use of IRX5183 in 1) patients with relapsed and/or refractory AML and 2) patients with high-risk MDS or chronic myelomonocytic leukemia (CMML).

NCT ID: NCT02749292 Terminated - Clinical trials for Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis

Maintenance of ANCA Vasculitis Remission by Intermittent Rituximab Dosing

MAINTANCAVAS
Start date: June 2016
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine the best management strategy to maintain remission in patients with ANCA vasculitis who have been treated with rituximab induced B cell depletion for at least two years. This study will compare intermittent B Cell depletion upon B cell return or intermittent B cell depletion upon serologic relapse.

NCT ID: NCT02748668 Terminated - Clinical trials for Extracorporeal Membrane Oxygenation

Extracorporeal Membrane Oxygenation (ECMO): Blood Cells

Start date: January 20, 2015
Phase:
Study type: Observational [Patient Registry]

The objective of the study is to predict outcomes of patients on extracorporeal membrane oxygenation (ECMO) therapy by correlating cytokines and inflammatory cell patterns to clinical outcomes using data collected in the ECMO Registry at Spectrum Health.

NCT ID: NCT02748564 Terminated - Metastatic Melanoma Clinical Trials

Aldesleukin and Pembrolizumab in Treating Patients With Stage III-IV Melanoma

Start date: March 21, 2017
Phase: Phase 2
Study type: Interventional

This study will evaluate the safety and tolerability of IL-2 when given in combination with pembrolizumab to patients with advanced melanoma. Aldesleukin may stimulate white blood cells to melanoma cells. Monoclonal antibodies, such as pembrolizumab, may interfere with the ability of tumor cells to grow and spread. Giving aldesleukin and pembrolizumab may kill more tumor cells. There are two parts to this study: - Phase Ib: To determine the safety and side effects of increasing doses of IL-2 in combination with pembrolizumab - Phase II: Once the maximum tolerated dose of IL-2 is determined, additional patients will be treated to determine if it is effective against the cancer.

NCT ID: NCT02745145 Terminated - Clinical trials for Systemic Sclerosis-associated Interstitial Lung Disease

Abituzumab in SSc-ILD

Start date: May 31, 2016
Phase: Phase 2
Study type: Interventional

The purpose of this trial was to compare two doses of abituzumab with placebo and determine whether abituzumab was more effective, safer, would be better tolerated and could provoke better immune response than placebo in the treatment of participants with SSc-ILD who already receive constant doses of mycophenolate.

NCT ID: NCT02740530 Terminated - Clinical trials for Executive Dysfunction

Improving Mobility and Cognition in Older Adults Using Non-Invasive Brain Stimulation

NIBS
Start date: April 2016
Phase: N/A
Study type: Interventional

This study aims to test the efficacy of a type of non-invasive brain stimulation (NIBS), known as repetitive transcranial magnetic (rTMS) stimulation, in improving mobility, particularly gait stability and variability, and executive dysfunction in older adults. The study will be conducted in forty older adults (≥60 years) with a diagnosis of executive dysfunction.