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NCT ID: NCT02653820 Not yet recruiting - Reflexology Clinical Trials

Complementary Effect of Reflexology on Chemotherapy-Induced Nausea and Vomiting

Start date: February 2016
Phase: Phase 2
Study type: Interventional

Reflexology treatment may influence the severity of chemotherapy-induced nausea and vomiting. This study aims to investigate the clinical effect of reflexology on chemotherapy-induced nausea and vomiting.

NCT ID: NCT02649413 Not yet recruiting - Clinical trials for Nephrotic Syndrome, Minimal Change

Adjusted Steroids Therapy in Childerens With Idiopathic Nephrotic Syndrome

AJSNS
Start date: March 2016
Phase: Phase 4
Study type: Interventional

The initial steroids dose for Nephrotic Syndrome is 60mg/1m2 for 6-4 weeks and the duration of the first steroid course is between 8 weeks to 6 months. The base of the initial dose for steroids Idiopathic nephrotic syndrome been put in the early 70s. In our study the investigators will adjusted the first steroids does to the response day. Our primary end point is : a lower adjusted dose is as good as the fix dose in the first year after diagnosis.

NCT ID: NCT02645110 Not yet recruiting - Hand Hygiene Clinical Trials

Evaluation of Effectiveness and Mildness of Whole-natural Hand-wash Formulations

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

The purpose of this study is to evaluate the effectiveness of whole-natural hand-wash formulations in bacterial removal and to estimate the relative mildness of the formulations.

NCT ID: NCT02644213 Not yet recruiting - Clinical trials for Physical Examination

Evaluation of Physical and Cognitive Performance After Simulated Road March Combines Physical and Cognitive Load Using a Virtual Reality Environment

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

The aim of the research is to evaluate the influence of physical and cognitive load as pre-mission activity on the soldier`s physical and cognitive performance, in compare to physical load alone. In order to do so, 12 healthy subjects will perform stimulated road march using a virtual reality environment combined with cognitive load and without, and their physical and cognitive performance will be evaluated by tests before and after.

NCT ID: NCT02641535 Not yet recruiting - Clinical trials for Physiological Stress

Evaluating the Physiological Strain Induced by a BC Membrane Protective Garment Under Exercise-heat Stress Compared to a Protective Coverall

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

Israel ministry of defense is examining a new BC membrane protective garment of BLAUER company constructed with GORE CHEMPAK fabric for the border guard of the police forces. The goal of this research is to perform a comparative experiment in order to evaluate the physiological strain induced by the new protective garment under exercise-heat stress conditions, compared to protective garment in current use.

NCT ID: NCT02641132 Not yet recruiting - Pterygium Clinical Trials

Pterygium Head Body MMC1: Two Different Surgical Procedures and Their Effect on Endothelial Cell Count.

PHB-MMC1
Start date: September 2015
Phase: Phase 4
Study type: Interventional

To evaluate changes in endothelial cell count after pterygium surgery with mitomycin C (MMC) 0.02%

NCT ID: NCT02631785 Not yet recruiting - Clinical trials for Pediatric Anxiety Disorders

Fear Conditioning, Extinction and Its Recall in Anxious Youth

FCPA
Start date: February 2016
Phase: N/A
Study type: Interventional

The proposed research aims to isolate brain-based information-processing mechanisms implicated in perturbed fear learning and extinction characteristic of pediatric anxiety. The study will focus on the therapeutic relevance of dysfunction in fear learning and extinction for treatment by examining the associations between brain functioning and response to exposure intervention in anxious children.

NCT ID: NCT02623231 Not yet recruiting - Depression Clinical Trials

The Effect of Escitalopram on Mood, Quality of Life and Cognitive Functioning in Glioblastoma Patients

Cipralex&GBM
Start date: December 2015
Phase: Phase 2/Phase 3
Study type: Interventional

Testing the effect of providing an antidepressant and anxiety-type escitalopram for patients with glioblastoma on patient's quality of life including the effect of treatment on mood and cognition during treatment.Two subgroups will fill questionnaires : - Questionnaire mini mental state exam (mmse) which is the maximum score of 30. A score of below 24 indicates a flaw in the level of dementia - Questionnaire depression / mood PHQ9P(Pa t i e n t H e a l t h Qu e s t i o n n a i r e - 9) - The M. D. Anderson Symptom Inventory (MDASI) - Evaluation of the hospital situation awareness (clinical assessment and questionnaire) - Cognitive assessment which will be carried out by the Department neuropsychological and include: - Executive function (Stroop) - Abstract Reasoning (similarities) - -Auditory and Spatial Attention (Digit span, Spatial span) visual memory and remembering Literature - Memory function - visual and auditory (ROCF, RAVLT) - Language function: Naming and verbal fluency - Mindstreems Neurotrax

NCT ID: NCT02621138 Not yet recruiting - Cerebral Palsy Clinical Trials

The Influence of Muscle Contraction on the Cardiac Autonomic System

Start date: April 2016
Phase: N/A
Study type: Observational

Population: 16 children with cerebral palsy, GMFCS 1-3.16 children typically developed, matched for age. All children aged 6-12 yrs who understand simple commands. Tools: 1. Polar monitor to record heart rate, attached to chest, in use throughout testing 2. Dynamometer- for assessing muscle strength. 3. Weights Method: Each child will be tested once. Both tools will be demonstrated and tried out before actual testing. With Polar watch attached: 1. 5 min sitting at rest, 2. knee muscle strength assessment with the dynamometer, 3. 15 minutes rest 4. Isometric and isotonic knee muscle contraction at 30% of childs` maximal strength as has assessed by the dynamometer. The child will asked to perform each for 3 minutes, with 5 minutes rest in-between All will be perform in both legs.

NCT ID: NCT02617524 Not yet recruiting - Aortic Stenosis Clinical Trials

Dedicated Sheath Feasibility Study

BAV
Start date: January 2016
Phase: N/A
Study type: Interventional

Dedicated Sheath feasibility study: A prospective, open-label study to evaluate the feasibility and safety of the Valve Medical Dedicated Sheath during Balloon Aortic Valvuloplasty (BAV).