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NCT ID: NCT02223949 Not yet recruiting - Obesity Clinical Trials

Labor Induction and Maternal BMI, Comparison of Different Pre-induction Cervical Ripening Methods

Start date: October 2014
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study is to investigate whether mechanical cervical ripening (using the Cook double balloon catheter) is superior or inferior to pharmacological agents (PGE1) in overweight and obese women undergoing labor induction.

NCT ID: NCT02223572 Not yet recruiting - Osteoporosis Clinical Trials

Secondary Fracture Prevention in Patients Who Suffered From Osteoporotic Fracture

Start date: September 2014
Phase: N/A
Study type: Interventional

Due to its prevalence worldwide, osteoporosis is considered a serious public health concern. The worldwide annual incidence of Osteoporotic fractures is approximately 2 million in the US only. Hip fracture is associated with serious disability and excess mortality. Studies have shown that an initial osteoporotic fracture is a major risk factor for a new fracture. An increased risk of 14.8% for a secondary hip fracture has been demonstrated in people that have already sustained a fracture in the past 4 years (In average). These data indicate the major opportunity afforded by secondary fracture prevention strategies. By responding to the first fracture, we can reduce the incidence of second and subsequent fractures. However, even after longer medical follow-up according to regular standard of care, medical treatment and rehabilitation, the medical system has been unable to translate the eminent risk into an effective preventive treatment.

NCT ID: NCT02222311 Not yet recruiting - Autism Clinical Trials

Influence of Vitamin D Deficiency on the Development of Autism

Start date: November 2014
Phase: N/A
Study type: Observational

The investigators wish to study the effect of Vitamin D on the development of autism in children. The investigators will also investigate the environmental and genetic influences on the level of Vitamin D in children with autism.

NCT ID: NCT02222012 Not yet recruiting - Depression Clinical Trials

Neuromarkers Identification in Major Depressive Disorder Based on Monitoring Measures

Start date: August 2014
Phase: N/A
Study type: Interventional

The investigators propose a multi-source pattern which integrates neuroimaging data associated with multiple, symptom-related neural processes relevant in depression to improve classification accuracy. The investigators conclude that combining brain activation related to the core-symptoms of depression using the multi-source monitoring data substantially increases classification accuracy while providing a sparse relational neuromarkers-model for future prediction.

NCT ID: NCT02221544 Not yet recruiting - Parkinson's Disease Clinical Trials

The Effect of Low-frequency rTMS on Motor Function in PD Patients With Freezing of Gait

Start date: September 2014
Phase: N/A
Study type: Interventional

This study is a double blind comparative study examining the effectiveness of the rTMS treatment on Freezing of Gait (FOG) phenomenon in patients with Parkinson's disease. We hypothesize that treatment using rTMS stimulation on frontal lobe areas will improve gait quality and decrease the frequency of FOG in patients with Parkinson's disease.

NCT ID: NCT02219867 Not yet recruiting - Clinical trials for Depressive Disorder, Major

Ketamine Infusions for Major Depression Disorder

Ketamie
Start date: August 2014
Phase: N/A
Study type: Interventional

Ketamine has been safely used for induction and maintenance of anesthesia for decades and more recently has been used for chronic pain. Ketamine is a noncompetitive, high-affinity antagonist of the N-methyl-D-aspartate type glutamate receptor, with additional effects on dopamine and μ-opioid receptors. During the last 9 years several uncontrolled reports have been published, showing a rapid and impressive effect of ketamine in TRD patients (Berman, Cappiello et al. 2000; Zarate, Singh et al. 2006; Mathew, Murrough et al. 2010; Aan Het Rot, Zarate et al. 2012; Mathew, Shah et al. 2012; Murrough, Iosifescu et al. 2013). Recently three placebo-controlled trials showed that a single dose of sub-anesthetic, (0.5 mg/kg) slow intravenous (IV) ketamine improves depressive symptoms dramatically. Across studies, a clinically significant antidepressant response was maintained for up to 72 hours in 12 of 25 patients. Nonetheless, all but two patients relapsed <2 weeks post-ketamine (Zarate, Singh et al. 2006; aan Het Rot, Zarate et al. 2012). Rot et al. showed that repeated IV ketamine infusions prolongs the duration of improvement. The investigators believe that the data presented above allows us to provide ketamine treatment here in the Sheba Medical Center for TRD patients.

NCT ID: NCT02218827 Not yet recruiting - Dry Eye Clinical Trials

Topical Steroid Treatment For Dry Eye

Start date: September 2014
Phase: N/A
Study type: Interventional

Many patients refer to an oculoplastic or corneal clinic examination due to dry eye symptoms. epidemiologic studies estimate that as many as 15% of the population over 60 years suffer from dry eye. the disease can be treated both topically through several drugs or through mechanical closure of the lacrimal drainage system. in the past decade a few studies demonstrated the efficacy of anti inflammatory treatment on dry eye disease due to the inflammatory process that occurs in it. this treatment rises goblet cell counts but in the meantime elevates the intra ocular pressure and elevates the risk for infections. steroids that cause a lower increase in intraocular pressure have not been thoroughly evaluated in dry eye disease. we with to subjectively and objectively evaluate an FDA approved topical steroidal drug in the treatment of dry eye.

NCT ID: NCT02216747 Not yet recruiting - Glomerular Disease Clinical Trials

Low Dose Steroids in the Treatment of Nephrotic Syndrome Relapse

NS
Start date: September 2014
Phase: Phase 4
Study type: Interventional

Background- Idiopathic Nephrotic syndrome is the common glomerular disease in childhood. conventional treatment is steroid treatment and nearly 90% response to this treatment well. Response to this treatment is the most important prognostic factor and this patients has a benign disease course. 60-70% among patients that response to steroid treatment,will suffer a relapse of NS.repeated steroids courses can lead to serious adverse events in children such as low bone density,weight gain ,growth slow down ,elevated blood pressure and eye pressure.there is side effect corelation between steroid dose and treatment duration. guidelines for steroid dose for NS relapse are not based on retrospective clinical research but only on Nephrologists and experts opinion. Rational- What would be the optimal low dose steroids and the shortest time of treatment in Nephrotic syndrome relapse?

NCT ID: NCT02214745 Not yet recruiting - Cerebral Palsy Clinical Trials

Demographic Characteristics of Children Suffering From Mental Retardation or Cerebral Palsy in the Israeli Arab Community

Start date: October 2014
Phase: N/A
Study type: Observational

To evaluate the demographic characteristics of patients suffering from mental retardation or cerebral palsy in the Israeli Arab community. Specific questionnaires will be developed and will be distributed amongst this population in order to identify these characteristics.

NCT ID: NCT02214680 Not yet recruiting - Healthy Clinical Trials

The Effect of Topical Treatment With Combigan Compared to Timolol and Brimonidine on Pupil Diameter

Start date: October 2015
Phase: Phase 2
Study type: Interventional

In this study we will explore the combined effect of Brimonidine and Timolol 0.5% (Combigan) eye drops on pupil dilation. It is a well studied phenoma that Brimonidine and a miotic effect on the pupil, however the combined effect of alpha agonist and beta blocker has not been studied.