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NCT ID: NCT00651339 Terminated - Cerebral Palsy Clinical Trials

The Effect of Botox Injection on Postural Stability of Cerebral Palsy (CP) Children

Start date: February 2008
Phase: N/A
Study type: Observational

Children suffer from Cerebral Palsy that willing to participate in the study will be tested with well-established measuring techniques of Balance control using force plate before 2 month after BOTOX injection in the movement and Rehabilitation Laboratory at BGU. An automated algorithm will be used to extract standardized stabilogram-diffusion parameters from each of the COP data sets collected during quiet standing. These parameters include diffusion coefficients, critical displacement, critical time and scaling exponents for both lateral and anterior-posterior sway directions (Collins & De Luca, 1993). Each of the Times (before 3 month and 6 month after the THA) in two task conditions (eyes closed and eyes close conditions). Participants will be required to stand on the platform 5 times for 30 s For each trial, they will be instructed to sway as little as possible. In addition Gait analysis will be also examined.

NCT ID: NCT00650897 Not yet recruiting - Diabetes Mellitus Clinical Trials

Efficacy Study of Escitalopram for Depression in Patients With Diabetes

EFDID
Start date: April 2008
Phase: Phase 4
Study type: Interventional

Patients with diabetes and major depression treated with Escitalopram might experience significant improvement in depression and anxiety scores; functional ability; diabetes-related self-care; and pain symptoms

NCT ID: NCT00650741 Enrolling by invitation - Clinical trials for Endothelial Dysfunction

Evaluation of a New Non-Invasive Device for Detection of Endothelial Dysfunction

Start date: February 2008
Phase: N/A
Study type: Observational

The purpose of the study is to investigate the sensitivity and specificity of the Endotect compared with an ultrasound device in a flow-mediated vasodilatation (FMD) test.

NCT ID: NCT00650676 Completed - Visual Impairment Clinical Trials

The Effect of Somatosensory Cue on Postural Stability in Blinded Persons

Start date: January 2008
Phase: N/A
Study type: Observational

Blind Adults that willing to participate in the study will be tested with well-established measuring techniques of Balance control using force plate in the movement and Rehabilitation Laboratory at Ben-Gurion University. An automated algorithm will be used to extract standardized stabilogram-diffusion parameters from each of the COP data sets collected during quiet standing. These parameters include diffusion coefficients, critical displacement, critical time and scaling exponents for both lateral and anterior-posterior sway directions (Collins & De Luca, 1993). the subjects will be tested in 3 task conditions (eyes blindfolded, eyes blindfolded holding stick, eyes blindfolded holding a dog). Participants will be required to stand on the platform 10 times for 30 s For each trial, they will be instructed to sway as little as possible.

NCT ID: NCT00649909 Completed - Clinical trials for Diabetes Mellitus, Type II

Effect of Glucose Control on the Response to Aspirin in Type 2 Diabetic Patients

Start date: November 2008
Phase: N/A
Study type: Observational

The efficacy of low dose aspirin appears to be substantially lower in diabetic patients, compared to patients without diabetes. We will perform an observational study where we follow up patients with uncontrolled type 2 Diabetes Mellitus and low response to aspirin (Aspirin Resistance), during a period of 6 months in the diabetic clinic. Our hypothesis is that glucose control will improve the response to aspirin in those patients.

NCT ID: NCT00648869 Withdrawn - Healthy Clinical Trials

Open-label Crossover Metformin Gum Versus Tablet in Healthy Volunteers

Start date: June 2008
Phase: N/A
Study type: Interventional

Single-dose, randomized, open-label, cross over study. The study will have an open-label, 3 period, 3 treatments, and randomized design. Each volunteer will receive a Metformin gum 2x250mg, Metformin gum 1x250mg & Metformin tablet 500mg

NCT ID: NCT00647374 Suspended - Fracture Clinical Trials

Assessment of Cortical Plasticity Following Short Term Limb Immobility

Start date: May 2008
Phase: N/A
Study type: Observational

The proposed project will study the consequence of short term limb immobility on the patterns of brain activity using functional imaging (fMRI)

NCT ID: NCT00647309 Recruiting - Hip Fracture Clinical Trials

Troponin Elevation in the Elderly Patient With Hip Fracture

Start date: April 2008
Phase: N/A
Study type: Observational

Elevated troponin is powerful and independent adverse prognostic marker in patient with ACS. However, non specific (non cardiac) troponin elevation is a common finding among hospitalized patients and worse prognosis too. The aim of this study is examine the prevalence of incidental cardiac troponin rise in a group of patient aged 65 and over admitted to geriatric department with hip fracture, and influence of troponin elevation on outcomes like ACS, death, motor and cognitive function.

NCT ID: NCT00646919 Not yet recruiting - Clinical trials for Staphylococcal Infections

Preoperative Nasal Swabs From Pediatric Patients

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

We intend to take a nasal swab from each pediatric pre-operative patient in our out-clinic with the intention of looking for a connection between positive operative incisions and a positive nasal swab. The patients will be in the out-patient clinic for a few hours, and will be examined post-operatively after one week. Those with positive nasal swabs will be advised to apply a nasal cream (Mupirocin)in their noses for one week. Our hypothesis is that there is a correlation between positive nasal swabs and positive incision infections.

NCT ID: NCT00646568 Completed - Infertility Clinical Trials

Human Chorionic Gonadotropin (hCG) Test: A Novel Method to Evaluate the Ovarian Reserve

Start date: June 2008
Phase: N/A
Study type: Interventional

In an era of delayed fertility plans, there is an increasing need for a reliable method to predict ovarian reserve and responsiveness. The current tests include serum FSH, Inhibin B, Mullerian inhibiting factor (MIF) and ultrasonographic measures such as ovarian volume and number of antral follicles are non-specific and with questionable reliability. The biochemical tests represent the function of production of androgens, as a predictor of ovarian reserve, has not been tested yet. Working hypothesis and aims: testing the prognostic capability of hCG stimulating test of theca cells for estimating the ovarian reserve, and by that to calculate better the chance for IVF cycle success