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NCT ID: NCT02504385 Not yet recruiting - Clinical trials for Developmental Coordination Disorder

The Effect of Virtual Reality on Motor Functioning and Participation Abilities Among Children With DCD

Start date: August 2015
Phase: N/A
Study type: Interventional

The subjet of this study is to explore the effect of using virtual reality environment at the clinic and at home (using Timocco) on the motor and participation abilities of children with DCD (Developmental Coordination Disorder). The study will examine the efficacy of using virtual reality gaming environment (Timocco) for treating children with DCD and the use of remote therapy, by shifting the focus of therapy from the clinic to the home environment, using the remote control system of Timocco for home practice.

NCT ID: NCT02507817 Not yet recruiting - Clinical trials for LIF LEVELS IN CORD BLOOD AND MATERNAL BLOOD DURING LABOR

Correlation Between LIF (Leukemia Inhibitory Factor ) Levels in Cord and Maternal Blood in Women Treated With Mg

Start date: August 2015
Phase: N/A
Study type: Observational

During embryonic development, there are several cytokines such as: LIF (Leukemia inhibitory factor), ciliary neurotrophic factor (CNTF), epidermal growth factor family (EGF), neuregulin 1 (NRG1) and transforming growth factor β (TGFβ) that were found are associated with neurogenesis and differentiation of brain cells. LIF is a cytokine that is essential for the development of the central nervous system, and has recently been shown in rats that maternal LIF stimulates placental ACTH (adrenocorticotropic hormone) that in turn promotes secretion of fetal LIF from nRBC (nucleated red blood cell ), which in turn promotes brain development of the fetus In other studies on rats a theory was proposed that LPS (lipopolysaccharide) and infection during pregnancy influence the normal development of the brain and may cause brain damage by altering placental ACTH thank in turn alters LIF secretion in the embryo which could be the cause of brain damage. Our hypothesis is that by treating the mother with Magnesium Sulphate we can protect the embryo's brain in one of two ways: 1. Altering Placental ACTH 2. Altering the number of receptors for LIF in the brain Women who are at risk for preterm labor prior to 32 weeks of gestation are treated with Magnesium Sulphate for neuroprotection, randomized controlled studies showed that if these women are treated in the 24 hours prior to labor with magnesium sulphate the risk for cerebral palsy and other severe motor problems are decreased. The mechanism for this decrease is unknown and that is the purpose of our study. The purpose of our research is to examine maternal LIF levels prior to birth and Maternal and cord levels after delivery and to see if levels are different if the mother was treated with Magnesium Sulphate. We will also check the placental ACTH level

NCT ID: NCT02508025 Not yet recruiting - Clinical trials for Musculoskeletal Diseases

Towards Better Understanding of FCE Performance in Different Societal Contexts

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Start date: August 2015
Phase: N/A
Study type: Observational

Purposes of this research: - To study similarities and differences in FCE performances between participants from different countries, jurisdictions, and evaluators. - To study determinants of FCE performance.

NCT ID: NCT02509715 Not yet recruiting - Thyroid Clinical Trials

Effect of Intraoperative Nerve Monitoring on Voice Quality During Thyroid Surgery

Start date: August 2015
Phase: N/A
Study type: Interventional

"Effect of intraoperative nerve monitoring on voice quality during thyroid surgery" Thyroidectomy is a quite often surgical procedure applied by both head and neck surgeons and endocrine surgeons.Recent advances in surgical and technological area achieve a remarkable decrease in the complication rates. In case of these advances, patients still have fear related with their voice. In this study, investigators aimed to investigate voice changes during thyroid surgery and effect of intraoperative nerve monitoring to the voice quality.

NCT ID: NCT02510586 Not yet recruiting - Moyamoya Disease Clinical Trials

Sevoflurane and Hyperperfusion Syndrome

Start date: August 2015
Phase: N/A
Study type: Interventional

The aim of the present study is to evaluate the effect of sevoflurane postconditioning on the incidence of postoperative hyperperfusion syndrome following revascularization surgery in moyamoya patients.

NCT ID: NCT02510612 Not yet recruiting - Diabetes Clinical Trials

Dexmedetomidine Affect Diabetic Patient's Glucose Metabolism

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Start date: August 2015
Phase: Phase 4
Study type: Interventional

Dexmedetomidine's Sedative Effect on Diabetic Patient

NCT ID: NCT02511548 Not yet recruiting - Circumcision, Male Clinical Trials

Increasing Medical Male Circumcision Uptake

Start date: August 2015
Phase: Phase 3
Study type: Interventional

The main objective of this study is to reach 80% circumcised men in a random sample of men living in the township of Orange Farm (South Africa).

NCT ID: NCT02511860 Not yet recruiting - Hypertension Clinical Trials

Burdock and Blood Pressure in African-American Women

Start date: August 2015
Phase: N/A
Study type: Interventional

This is a study of women aged 18-65, to determine the physiological effects of consuming burdock root in supplement form. Burdock has long been used by herbalists for its diuretic and blood sugar lowering properties.

NCT ID: NCT02513082 Not yet recruiting - Osteoarthritis Clinical Trials

Effectiveness of Pain Relief Between Adductor Canal Block and Femoral Nerve Block in Total Knee Arthroplasty

Start date: August 2015
Phase: N/A
Study type: Interventional

This study aims to compare the effectiveness of adductor canal block and femoral nerve block in total knee arthroplasty in general anesthesia. Two block techniques were proved safe and effective in pain control after total knee arthroplasty. But some authors insist that quadriceps muscle power was decreased by femoral nerve block. The study design is a double-blind randomized controlled trial. Fifty patients planed to undergo simultaneously bilateral total knee arthroplasty are randomised to receive ultrasound-guided femoral nerve block on one leg and adductor canal block on the other, in addition to combined general anaesthesia. The primary outcome was comparative postoperative pain in either extremity at four, eight, 12, 24, 72 hours and 7days postoperatively. Secondary comparative outcomes included motor strength by cybex test.

NCT ID: NCT02515409 Not yet recruiting - Clinical trials for Sleep Apnea, Obstructive

Heated Humidified High Flow Nasal Cannula for Children With Obstructive Sleep Apnea

Start date: August 2015
Phase: N/A
Study type: Observational [Patient Registry]

The purpose of this study is to determine whether heated humidified high flow nasal cannula (HHHFNC) is effective as a treatment of obstructive sleep apnea syndrome (OSAS) compared to continues positive airway pressure (CPAP) treatments in children and to compare their adherence and compliance.