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NCT ID: NCT01629147 Not yet recruiting - Constipation Clinical Trials

Treatment of Chronic Constipation in Children With Lactobacillus Reuteri

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

Lactobacillus reuteri (Biogaia) may be beneficial for treatment of chronic constipation in children 4-10 years of age.

NCT ID: NCT01626521 Not yet recruiting - Clinical trials for Chronic Obstructive Pulmonary Disease

Value of Prothrombin Fragment F1+2 in the Diagnosis of Pulmonary Embolism in Patients With Chronic Obstructive Pulmonary Disease (COPD) Exacerbation

Start date: July 2012
Phase: N/A
Study type: Observational

To access the clinical usefulness of F1+2 in the diagnosis of PE in patients with AECOPD who require hospitalization. Specifically, to determine whether F1+2 may have an additional value in the subgroup of patients with an abnormal D-dimer,to determine whether it may increase the proportion of patients in whom PE can be safely ruled out and to determine the sensitivity, specificity and NPV of F1+2 at various cut-off values.

NCT ID: NCT01623921 Not yet recruiting - Clinical trials for Acute Respiratory Distress Syndrome

Statins and Selective Cyclooxygenase-2 Receptor Inhibitors in Blunt Chest Trauma

Start date: August 2012
Phase: N/A
Study type: Interventional

Background: Lung contusion affects 17%-25% of adult blunt trauma patients, and is the leading cause of death from blunt thoracic injury. Statins are lipid-lowering drugs with recently suggested anti-inflammatory and antioxidant properties. Cyclo-oxygenase-2 (COX-2) is a key enzyme in the production of prostaglandins (PG), and evidence suggests that COX-2 plays an important role in the pathogenesis of acute lung injury (ALI). Aims: The current study aims at evaluating the beneficial effects of statins and COX-2 receptor inhibitors on ALI elicited by blunt trauma to the chest. Methods: After approval by the institutional ethics and a scientific committee, and obtaining informed consent , patients admitted to the emergency department (ED) due to blunt trauma with a diagnosis of lung contusion will be enrolled in the study.The effects of statins and COX 2 inhibitors on ALI will be assessed by recording clinical parameters and measuring inflammatory mediators levels in the serum and in the bronchoalveolar space. Expected results: The investigators expect to find that the proposed treatment will be effective in reducing ALI burden. The investigators also suppose that using a combination of those drugs will synergistically potentiate their effect on ALI.

NCT ID: NCT01621620 Not yet recruiting - Pain Clinical Trials

The Role of Sympatho-vagal Balance on Different Limbs of Pain Perception in Healthy Subjects

Start date: August 2012
Phase: N/A
Study type: Interventional

objectives 1. To study the sympatho-vagal balance effect on different limbs of pain perception. 2. To determine whether it is the hypertension by itself or the baroreflex activation due to blood pressure rise that is responsible for the analgesic effect of acute hypertension. study questions The study questions are derived from the study objectives: 1. Does sympatho-vagal balance influence pain perception? 2. Does sympatho-vagal balance influence diffuse noxious inhibitory control systems? 3. Does sympatho-vagal balance influence temporal summation? 4. Does the hypoalgesic effect to acute increase in blood pressure a result of baroreflex activation?

NCT ID: NCT01618110 Not yet recruiting - Clinical trials for Attention Deficit/Hyperactivity Disorder

Transcranial Magnetic Stimulation in Treatment of Attention Deficit/Hyperactivity Disorders

Start date: July 2012
Phase: N/A
Study type: Interventional

- ADHD is one of the most common psychiatric disorders. - While most of the attention is directed towards youth, 60% continue to suffer symptoms into adult life. - Current treatment is effective, but 30% suffer side effects that lowers QOL, and 20% are non-responders. - Known mechanism of pathophysiology includes hypoactive dopaminergic system, especially at right PFC. - It is this study hypothesis that by stimulating the right PFC by TMS, it will be possible to alleviate ADHD symptoms. - A 10 sessions of treatment will by applied on a randomly allocated group of patients, diagnosed with ADHD, in a 2:1 ratio: The first group will receive an actual TMS treatment, and the second group will receive a sham treatment. - Improvement of objective and subjective ADHD scale will be examined.

NCT ID: NCT01616004 Not yet recruiting - Pain Clinical Trials

Effect of Acute Treatment With N2O on Inhibitory Pain Mechanisms in Healthy Subject

N2O
Start date: October 2014
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether N2O (laughing gas) has an antinociceptive effects in healthy volunteers.

NCT ID: NCT01615848 Not yet recruiting - Clinical trials for Polycystic Ovary Syndrome

Comparison Between Mediterranean Diet and High Protein Diet in Women With Polycystic Ovary Syndrome (PCOS)

Start date: April 2013
Phase: N/A
Study type: Interventional

Polycystic ovary syndrome (PCOS) affects 5-10% of women and is the most common endocrine syndrome.PCOS is associated with infertility, risk for obesity and type 2 diabetes. The elevated insulin characteristic of PCOS is likely to play a major role in its symptoms. restricted calorie High protein diet and mediterranean diet may improve insulin sensitivity and therefore lower androgen production in women with pcos women.the purpose of this study is to determine which diet is more effective in improving metabolic and reproductive outcomes.

NCT ID: NCT01615107 Not yet recruiting - Clinical trials for Cervix; Insufficient Dilatation in Labor

Premature Rupture of Mambrane and Unfavourable Cervix

Start date: July 2012
Phase: N/A
Study type: Interventional

The paucity of published data concerning the issue of mechanical labor induction in the setting of Term PROM has led us to undertake the present clinical trial. This study is designed to compare the efficacy and safety of the standard Oxytocin induction protocol with the double-balloon catheter device with concurrent oxytocin administration in patients with Term PROM and unfavorable cervical conditions.

NCT ID: NCT01614236 Not yet recruiting - Clinical trials for Multimodal Analgesia

Pre- Versus Post-Incisional Pregabalin for Postoperative Pain Control

Start date: July 2012
Phase: N/A
Study type: Interventional

Proper pain relief is a major concern of patients worldwide. Preoperatively, one of the most common questions asked by patients pertains to the amount of pain they will experience after surgery how long it will last and how good will it be controlled. Pain concerns the surgical team as well, because of its correlation with clinical outcomes and patients' satisfaction rate . Studies have shown that negative clinical outcome with regard to pain control includes decreases in vital capacity and alveolar ventilation, pneumonia, tachycardia, hypertension, myocardial ischemia, transition into chronic pain, poor wound healing, and psychological sequelae .

NCT ID: NCT01609699 Not yet recruiting - Clinical trials for Reduction in Abdominal Circumference

Effectiveness Study of the UltraShape® Contour I-Y for Non-Invasive Reduction in Abdominal Circumference

Start date: August 2012
Phase: N/A
Study type: Interventional

The UltraShape® Contour I- Y system uses focused ultrasound to produce localized mechanical motion within fat tissues and cells for the purpose of producing mechanical cellular membrane disruption. It is intended for reduction in body circumference. The primary objective of this study is to evaluate the efficacy of the Contour I - Y System on abdominal circumference reduction relative to baseline pretreatment values using different treatment methods. The primary efficacy endpoint in this trial is Statistical Difference of Circumference reduction between Baseline measurement and at follow-up measurement.