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NCT ID: NCT01104311 Active, not recruiting - Brain Ischemia Clinical Trials

Strategy for Adequate Blood Pressure Lowering in the Patients With Intracranial Atherosclerosis

STABLE-ICAS
Start date: April 2010
Phase: Phase 4
Study type: Interventional

To develop adequate blood pressure (BP) lowering strategy after subacute ischemic stroke patients with symptomatic severe intracranial atherosclerosis. Primary hypothesis of this study is that aggressive BP control (lowering systolic BP between 110mmHg and 120mmHg) will not increase the ischemic lesion volumes in hemisphere compared to modest BP lowering (lowering systolic BP between 130mmHg and 140mmHg) in the patients with symptomatic severe intracranial atherosclerosis.

NCT ID: NCT01104350 Active, not recruiting - Bladder Cancer Clinical Trials

Image-Guided Radiation Therapy for Bladder-Cancer Patients Undergoing Radiotherapy and Concurrent Gemcitabine Chemotherapy

Start date: April 2010
Phase: Phase 1
Study type: Interventional

The purpose of this study is to test the safety of different amounts (doses) of external radiation therapy (high-energy x-rays that shrink or destroy cancer) combined with chemotherapy.

NCT ID: NCT01104571 Active, not recruiting - Breast Cancer Clinical Trials

Trastuzumab or Lapatinib Ditosylate in Treating Women With Early Breast Cancer

EPHOS-B
Start date: April 2010
Phase: Phase 3
Study type: Interventional

RATIONALE: Monoclonal antibodies, such as trastuzumab, can block tumor growth in different ways. Some block the ability of tumor cells to grow and spread. Others find tumor cells and help kill them or carry tumor-killing substances to them. Lapatinib ditosylate may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. It is not yet known whether trastuzumab or lapatinib ditosylate is more effective in treating women with early breast cancer. Update June 2013: Since the initial development of EPHOS-B in 2007 more evidence in relation to safety and efficacy of anti-HER2 therapies are now available, and in particular, a growing body of evidence that combinations of two anti-HER2 therapies are more effective than monotherapies. Therefore this study has been amended (PART 2) to a 1:1:2 ratio to control, perioperative trastuzumab or the combination of lapatinib and trastuzumab. PURPOSE: This randomized phase III trial is studying trastuzumab to see how well it works compared with lapatinib ditosylate (and in since June 2013 - compared with a combination of lapatinib and trastuzumab) in treating women with early breast cancer.

NCT ID: NCT01104857 Active, not recruiting - Sepsis Clinical Trials

Respiratory Muscle Dysfunction in Critically Ill Patients

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

Respiratory muscle dysfunction in critically ill patients is associated with elevated morbidity, including prolonged weaning from mechanical ventilation. The causes for respiratory muscle dysfunction in these patients is poorly understood and no effective treatment is available. The general hypothesis of the present study is that in critically ill mechanically ventilated subjects respiratory muscle dysfunctions results from loss of myosin induced by activation of proteolytic cascades.

NCT ID: NCT01109108 Active, not recruiting - Clinical trials for Nasopharyngeal Carriage of S. Pneumoniae

Streptococcus Pneumonia: Effects of PCV13 on Pneumococcal Carriage

Start date: April 2010
Phase: N/A
Study type: Observational

The specific aim is to evaluate the impact of PCV13 as administered in the pediatric primary care clinic at Boston medical center on the serotype specific carriage of Streptococcus pneumoniae in children < 5 and their parents. Specifically the investigators will measure the decline in vaccine serotypes, the proportion of children receiving vaccine required to achieve 50% reduction in serotype specific carriage and the correlation between immunogenicity of the specific serotypes and decline in carriage.

NCT ID: NCT01111435 Active, not recruiting - Spasticity Clinical Trials

A Prospective Study of Spasticity in Individuals With Multiple Sclerosis

Start date: April 2010
Phase: N/A
Study type: Observational

This study is expected to contribute to the body of knowledge on the benefits of individuals with MS taking glatiramer acetate (Copaxone®). If patients have less spasticity when taking glatiramer acetate (Copaxone®), they may be more likely to have an improved quality of life. The hypotheses for this study are: 1. Study participants who transition from interferon therapy to glatiramer acetate (Copaxone®) for a six month period will have a decrease in spasticity. 2. Study participants who transition from interferon therapy to glatiramer acetate (Copaxone®) for a six month period will have a change in perceptions of the impact of spasticity on their lives.

NCT ID: NCT01112072 Active, not recruiting - Keratoconus Clinical Trials

Corneal Collagen Crosslinking and Intacs for Keratoconus and Ectasia

CXL
Start date: April 2010
Phase: Phase 3
Study type: Interventional

This study will determine the efficacy of corneal collagen crosslinking (CXL) combined with Intacs for the treatment of keratoconus and corneal ectasia. The goal of CXL is to decrease the progression of keratoconus, while Intacs has been shown to decrease corneal steepness in keratoconus. This study will attempt to determine the relative efficacy of the two procedures either performed at the same session versus CXL performed 3 months after Intacs.

NCT ID: NCT01115868 Active, not recruiting - Scarring Clinical Trials

Prevascar in African Continental Group Scarring

Start date: April 2010
Phase: Phase 1
Study type: Interventional

There is considerable variation in scarring, within and between people, and between different ethnic groups. Individuals with more pigmented skin are more prone to severe scarring than those traditionally termed white. Prevascar is being developed by Renovo for use as a potential treatment for reducing scarring. Renovo's histological analysis of wounds and scars in human non drug studies demonstrates an increase in wound and scar width in subjects of African Caribbean ancestry over a 12 month period. It is hypothesised that IL-10 may be a potentially beneficial therapy for the reduction of scarring in Non Caucasians of African-Caribbean ancestry. This Renovo clinical trial will be carried out primarily to establish the effects of four doses of Prevascar on 1cm incisional and excisional scars in subjects of African Continental Group ancestry, as compared to placebo, and to further investigate the safety and tolerance of intradermally injected Prevascar in wounds.

NCT ID: NCT01137227 Active, not recruiting - Obesity Clinical Trials

Factors Associated With Physical Inactivity Among Adolescents

FAPIA
Start date: April 2010
Phase: N/A
Study type: Observational

Despite the acknowledgment that physical activity is important for health, there are still few population-based or school-based studies that uses the current physical activity guidelines for adolescents. Physical inactivity was defined a less than 300 min/w of moderate to vigorous-intensity physical activity practice. Previous research has shown very high prevalence rates of physically inactive adolescents and a strong association with demographic, socioeconomic and biological factors. Based on this information, the investigators are elaborating a systematic review of literature to obtain and provide more accurate information in this context.

NCT ID: NCT01144390 Active, not recruiting - Heroin Dependence Clinical Trials

Effect Study of Optimized Intervention to Heroin Addicts

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

The purpose of this study is to explore barriers and determine whether optimizing protocol is effective in the treatment of heroin dependence in community-based MMT clinics.