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NCT ID: NCT02384694 Completed - Metabolic Syndrome Clinical Trials

Effects of a Zumba Dance Program for Postmenopausal Women With Metabolic Syndrome

ZumBeat
Start date: May 2014
Phase: N/A
Study type: Interventional

The aim of this study is to examine the effects of a 12-week Zumba dance intervention on fitness, anthropometric and psychometric parameters and eating behavior.

NCT ID: NCT02384616 Completed - Hyperoxia Clinical Trials

Hyperoxygenation in Anesthetized Children

OXPED
Start date: May 2015
Phase: N/A
Study type: Interventional

This study is aiming at assessing the effect of inspired oxygen fraction during general anesthesia on children's lung mechanics and volume. More specifically, the temporal change in end-expiratory lung volume (EELV) and respiratory system resistance and elastance during the perioperative period will be characterized in order to define the the effect of high inspired fraction of oxygen on lung function.

NCT ID: NCT02384538 Completed - Hand Osteoarthritis Clinical Trials

A Phase 2a Study Evaluating the Safety and Efficacy of ABT-981 in Patients With Erosive Hand Osteoarthritis

Start date: July 2013
Phase: Phase 2
Study type: Interventional

This is a multicenter, randomized, double-blind, placebo-controlled study to compare the safety and efficacy of ABT-981 to placebo in subjects with erosive hand osteoarthritis.

NCT ID: NCT02384148 Active, not recruiting - Obesity Clinical Trials

Study of Circadian Clock Properties in Healthy Subjects, Obese and Type 2 Diabetic Patients.

Start date: June 2011
Phase: N/A
Study type: Observational

The investigators aimed to characterize human circadian clockwork in healthy individuals in comparison to obese and type 2 diabetic subjects, employing the noninvasive experimental approach allowing the study of circadian profile in human individuals.

NCT ID: NCT02384135 Recruiting - Clinical trials for Deep Vein Thrombosis

Age-adjusted D-dimer Cutoff Levels to Rule Out Deep Vein Thrombosis: a Prospective Outcome Study

ADJUST-DVT
Start date: March 2015
Phase: N/A
Study type: Interventional

Prospective validation of an age-adjusted D-dimer cut-off to rule out deep vein thrombosis (DVT)

NCT ID: NCT02383680 Recruiting - Clinical trials for Dermatologic Disorders

Yellow Fever Vaccination Under Low Dose Methotrexate Therapy

MTX_YF
Start date: December 2014
Phase: N/A
Study type: Observational

Travelers (n = 30, 15 taking low-dose methotrexate (MTX), 15 healthy controls (HC), seeking travel advice in one of the following Swiss Travel Centers (Aarau, Basel, Bern, Geneva, Lausanne, Zurich) and who have an indication for yellow fever (YF) vaccination according to the Swiss Federal Office of Public Health's vaccination recommendations are invited to participate in this study. After signing the consent form (i) YF viremia and (ii) anti-YF antibody production in patients taking low-dose MTX and HC will be compared after YF vaccination. It will be analyzed whether the percentage of people with protective antibodies differs between the two groups and (iii) vaccine side effects will be compared between the groups.

NCT ID: NCT02383147 Completed - Clinical trials for Tinnitus, Subjective

Efficacy Study for Development and Use of Neurofeedback-trainings for Patients Suffering From Chronic Tinnitus

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

Chronic tinnitus affects about 10-15% of the population in industrialized countries. Investigations of the brain activity by using electroencephalography (EEG) showed that in localized regions of the hearing system brain activity was decreased. This reduction of activity is thought to be one of the reasons that keep the perception of the tinnitus going. Recent studies have shown that neurofeedback is a viable option for treatment of chronic tinnitus. By using neurofeedback it is possible to train brain functions by the simple principle of rewarding wanted changes and punishing unwanted ones. The purpose of the investigators study is to show the efficacy of specific localized neurofeedback training in comparison to global relaxing neurofeedback training. In order to achieve decreased tinnitus symptoms or even disappearance of the tinnitus, 15 neurofeedback trainings are planned. Before and up to 6 month after the training EEG-recordings are performed.

NCT ID: NCT02383108 Completed - HIV Infection Clinical Trials

Strategy for Maintenance of HIV Suppression With Once Daily Integrate Inhibitor+Darunavir/Ritonavir in Children

SMILE
Start date: June 2016
Phase: Phase 2/Phase 3
Study type: Interventional

A two-arm, Phase 2/3 multicentre, open-label, randomised study evaluating safety and antiviral effect of current standard antiretroviral therapy compared to once daily integrase inhibitor administered with darunavir/ritonavir (DRV/r) in HIV-1 infected, virologically suppressed paediatric participants.

NCT ID: NCT02382887 Completed - Spinal Injuries Clinical Trials

Comparison by Neuromonitoring of Two Techniques of Tracheal Intubation in Patients With Unstable Cervical Spine

Start date: March 2009
Phase: N/A
Study type: Interventional

Patients who present with an unstable cervical spine following an accident need a general anesthesia for the necessary surgery. Commonly, the management of the tracheal intubation is performed by a fiberoptic technique. However, changes in equipment availability and quality may challenge the fiberoptic intubation technique. The investigators wish to compare the tracheal intubations performed with the Airtraq in comparison with the fiberscopic technique.

NCT ID: NCT02382692 Completed - Clinical trials for Cerebrospinal Fluid Leakage

Cerebrospinal Fluid Rhinorrhea After Functional Endoscopic Sinus Surgery

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

Sinus surgery is a common procedure. A potential complication is injuring the membranes of the brain. This can lead to leakage of brain fluid through the nose. We would like to estimate the incident rates of that complication. At the end of the operation, a thin gauze is inserted into the nose on both sides in addition to the usual tampon. This gauze will be analyzed at the laboratory for beta-2-transferrin, which is a biomarker for brain liquid.