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NCT ID: NCT00305513 Not yet recruiting - Clinical trials for Cerebrovascular Accident

Effectiveness of Rehabilitation on the Recovery of Patients Post Right Stroke With Unilateral Spatial Neglect

Start date: n/a
Phase: Phase 2
Study type: Interventional

Unilateral spatial neglect (USN) is believed to be a disorder of attention, characterized by impairment in the ability to perceive or respond to stimuli presented to the contralesional space, and which is not attributable to significant sensory or motor deficits. USN has serious consequences for rehabilitation and long term disabilities. Efforts have been made to clarify both the theoretical basis of this phenomenon and the rehabilitation methods that will be best in improving function. The purpose of this study is to try and contribute to both efforts by examining treatment effectiveness of two methods; one targeting general arousal (phasic alerting), and the other targeting increasing awareness to left side stimuli and habit changes. Functional neuroimaging methods (PET [positron emission tomography] and fMRI [functional magnetic resonance imaging]) have been applied to understand the functional anatomy of the brain during mental processes. Only a few attempts have been made to use functional neuroimaging in patients with neurological deficits such as USN, usually speculations are made based on findings with healthy participants to explain this disorder. This study's aim is to examine the functional reorganization of the attentional network in the brain of USN patients while performing visual tasks, by means of functional neuroimaging techniques, in light of specific rehabilitation techniques. Patients will be examined before and after 3 weeks of rehabilitation both using standardized neurobehavioral tests and PET imaging procedures.

NCT ID: NCT00309673 Not yet recruiting - Tuberculosis Clinical Trials

Local Anesthesia and Tuberculin Skin Test in Infants and Children

Start date: n/a
Phase: N/A
Study type: Interventional

The use of local anaesthesia efficiently reduces pain due to needle puncture. However, when tuberculin skin test is performed it is the skin reaction to tuberculin injection that is studied. It is a quantitative skin reaction measured in millimiters. From the study of literature it is not known whether local anaesthetic modify skin reaction to tuberculin. Therefore, before recommending the use local anaesthesia for tuberculin intradermal injection we have to rule out a potential effect of local anaesthetic on the result of the test. This is particularly important in children, since there are more sensitive to pain than adults

NCT ID: NCT00311285 Not yet recruiting - Stress Clinical Trials

Physical and Mental Load in the Surgeon Performing Laparoscopic Tasks

Start date: n/a
Phase: N/A
Study type: Interventional

The surgeons load during laparoscopic surgery is still unclear. Laparoscopic surgery is more demanding because of the challenge of operating through small scars in the abdominal wall without any tactile feedback depending only on the visual feedback on a monitor. The purpose is to establish a model of how to measure mental and physical load in laparoscopy.

NCT ID: NCT00318162 Not yet recruiting - Clinical trials for Pervasive Developmental Disorder

Trial of Low-Dose Naltrexone for Children With Pervasive Developmental Disorder (PDD)

Start date: n/a
Phase: Phase 1/Phase 2
Study type: Interventional

This study will examine the effects of low-dose naltrexone (LDN) on children with autistic spectrum disorders. The investigators hope to show a positive effect on social functioning and language.

NCT ID: NCT00318513 Not yet recruiting - Lymphedema Clinical Trials

Safety Study of Bevacizumab to Treat Women With a History of Breast Cancer and Suffering From Upper Extremity Lymphedema

Start date: n/a
Phase: Phase 1
Study type: Interventional

The purpose of this study is to determine the safety and side effects of bevacizumab in subjects with lymphedema who will initially receive bevacizumab alone and then in combination with standard manual lymphatic drainage (MLD) and combined decongestive therapy (CDT). This study will help to determine the dose of bevacizumab to be used in future studies of subjects with lymphedema.

NCT ID: NCT00318604 Not yet recruiting - Clinical trials for Head and Neck Cancer

Plasma Circulating Deoxyribonucelic Acid (DNA) as a Response Marker

Start date: n/a
Phase: N/A
Study type: Observational

This study investigates whether the amount of circulating plasma DNA can be used as a response marker for anti-cancer treatment in treating gross tumors.

NCT ID: NCT00319293 Not yet recruiting - Clinical trials for Polycystic Ovary Syndrome

Efficacy of Metformin in Lean Women With Polycystic Ovary Syndrome

Start date: n/a
Phase: N/A
Study type: Interventional

Insulin resistance is an important feature of the polycystic ovary syndrome,and patiens are successfully treated with the insulin sensitizing agent metformin. The insulin resistance of lean patients with the syndrome is debated. In this study, we will study the change in insulin resistance, metabolic and hormonal factors after 3 months of metformin treatment in lean PCOS women.

NCT ID: NCT00334477 Not yet recruiting - Clinical trials for Erectile Dysfunction

Efficacy and Safety of Tadalafil in Hemodialysis Patients

Start date: n/a
Phase: Phase 2
Study type: Interventional

The purpose of this study is to check the safety and efficacy of a pde5 inhibitor, tadalafil, is a special group of patients: Renal chronic patients in hemodialysis treatment.

NCT ID: NCT00338819 Not yet recruiting - Ventilated Patients Clinical Trials

ActiveCare+SFT Hemodynamic Profile Compare to SCD Express in Ventilated Patients

Start date: n/a
Phase: N/A
Study type: Observational

Purpose: To test the hemodynamic profile generated by the MCS’s ActiveCare+SFT device in ventilated patients and compare it to that of the Kendall SCD Express. Design: Comparative, prospective study. Patients are their own controls.

NCT ID: NCT00339118 Not yet recruiting - Rhabdomyosarcoma Clinical Trials

EpSSG (European Soft Tissue Sarcoma Study Group) Protocol for Non-Metastatic Rhabdomyosarcoma in Children

Start date: n/a
Phase: Phase 4
Study type: Interventional

The purpose of the study is achieve standardization treatment of low and intermediate risk rhabdomyosarcoma patients, with an attempt to improve treatment results in high and very high risk patients by the addition of doxorubicin as induction treatment and at the maintenance phase.