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NCT ID: NCT04114539 Completed - Clinical trials for Tourette Syndrome in Adolescence

Ecopipam Tablets to Study Tourette Syndrome in Children and Adolescents - Open Label Extension

Start date: October 4, 2019
Phase: Phase 2
Study type: Interventional

This study was an international, multicenter, open-label, long term extension study evaluating the safety of ecopipam tablets for the treatment of children and adolescent subjects with Tourette Syndrome.

NCT ID: NCT04114435 Recruiting - Clinical trials for Prematurity; Extreme

Pulmonary Vascular Disease and Cardiac Performance in Extreme Preterm Infants

Start date: October 12, 2019
Phase:
Study type: Observational

Pulmonary vascular disease and cardiac performance in extreme preterm infants: A prospective cross-sectional study

NCT ID: NCT04114045 Completed - Inflammation Clinical Trials

Effects of Post-exercise Protein Supplementation in Young Athletes

Start date: December 19, 2016
Phase: N/A
Study type: Interventional

This randomised double blind, placebo-controlled study examined the effects of post-exercise consumption of whey protein (PRO) or carbohydrate (CHO) on performance recovery, muscle damage and inflammatory cytokine responses following a high intensity interval swim (HIIS) in 10-17-year old male and female swimmers.

NCT ID: NCT04113681 Recruiting - Clinical trials for Osteoarthritis, Knee

Pilot Study: Geniculate Artery Embolization in Knee Osteoarthrosis.

Start date: February 14, 2019
Phase: N/A
Study type: Interventional

Geniculate Artery Embolization (GAE) has recently been described and studied as a palliative treatment for osteoarthrosis-related knee pain in patients un-eligible for surgical intervention. This treatment is based on the hypothesis that hypervascularization and associated increased nerve proliferation are possible sources of chronic pain following the morphological changes of osteoarthrosis. A large animal model has shown digital subtraction arteriography to be well correlated to both the histological findings of synovial inflammation and synovial contrast enhancement on magnetic resonance imaging. This embolization technique has also been applied to other regions of the musculoskeletal system including the elbow and the shoulder.

NCT ID: NCT04113538 Active, not recruiting - Clinical trials for Wet Age-related Macular Degeneration

Treat and Extend Analysis Trial With Aflibercept in Wet-AMD

Start date: July 24, 2019
Phase: Phase 3
Study type: Interventional

This study is a randomized, prospective, exploratory, descriptive, open label, parallel group, post-authorization study designed to describe and evaluate two aflibercept treatment regimens aimed at achieving and maintaining a maximum visual function benefit (i.e., BCVA stability). The goal of the study is to compare two strategies for dosing regimen with aflibercept in wet AMD: the standard regimen (one injection every 8 weeks after 3 monthly loading doses in the treatment of wet age-related macular degeneration) versus the treat and extend protocol (details outlined below in the "Study Design" section) aiming at achieving and maintaining maximum visual acuity benefit while minimizing the number of injections. Patients will be randomized at week 8 (Month 2) in a proportion of 1:2 (Standard treatment : treat and extend treatment). We aim to demonstrate that the Treat and Extend regimen is equivalent or better to the standard fixed interval regimen in terms of change in patients' visual acuity after a year of treatment and that patients in the Treat and Extend arm will receive fewer injections and fewer visits, than their counterparts in the standard regimen arm. The results could be used to generate a base for future controlled-randomized clinical trials on the timing of treatment administration for patients with wAMD.

NCT ID: NCT04112940 Completed - Clinical trials for Deglutition Disorders

Physiological Flow of Liquids in Head and Neck Cancer Patients: A Pilot Study

Start date: December 19, 2016
Phase:
Study type: Observational

This study is part of a larger grant, for which the overall goal is to collect measurements of liquid flow through the oropharynx (i.e., mouth and throat) during swallowing. The focus of this study is to evaluate the flow of liquids of varying consistency in the head and neck cancer population.

NCT ID: NCT04112927 Recruiting - Clinical trials for Obstructive Sleep Apnea

Acoustic OSA Prediction During Wakefulness and Monitoring During Sleep

Start date: October 1, 2021
Phase:
Study type: Observational

The purpose of this study is to investigate the feasibility of sound analysis for: a) sleep apnea detection both during wakefulness and sleep, and b) flow-sound relationship during both wakefulness and sleep in patients and control individuals. The ultimate goal of our research is to simplify the current assessments for sleep apnea detection so that it is more convenient for patients and also much faster than the current techniques.

NCT ID: NCT04112459 Recruiting - Clinical trials for Prolonged Mechanical Ventilation in Pediatric Intensive Care Unit

LongVentKids Study

LVK
Start date: September 4, 2019
Phase:
Study type: Observational

Scientific advances, population growth, lower mortality, and increasing complexity of diseases have boosted up the number of patients requiring prolonged breathing assistance with mechanical ventilators in the pediatric intensive care units (PICU) in many parts of the developed world. Previous studies also suggest that there is a small group of children who actually need such a high level of support for extended periods of time, utilizing a lot of human and technical resources. We defined children with prolonged mechanical ventilation (PMV) if they required supports with a breathing machine for more than 14 days. We propose an international point prevalence study of children requiring PMV in PICU. We will conduct the study in multiple centers in several different regions, including North and South America, Europe, and Asian countries, with a strong relationship with local physician colleagues. Practice for patients requiring PMV will be examined including the type and size of local PICU, admission and discharge policies, and patient and treatment modalities administered to such patients, types of professionals looking after patients in PMV, types of health care. We anticipate a high variability in practices suggesting a need to further standardize the management of PMV.. Specifically, as an immediate consequence, by comparing and understanding the differences in patient demographics, practice details among PICUs in regards to the background factors of local PICUs and their patients, practitioners will share their way of dealing with such patients. In that way, this study will support the need to generate guidelines and lead to patient care improvement in PICUs.

NCT ID: NCT04111718 Recruiting - Clinical trials for Osteoarthritis, Knee

The Impact of Procedural Awareness of Knee Injections for Osteoarthritis on Patient Perceptions of Effectiveness

Start date: October 1, 2019
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine whether outcomes for patients receiving intra-articular platelet-rich plasma (PRP) injections for knee osteoarthritis are influenced by observation of the preparatory steps to the procedure. The viewing of the steps involved in the administration of PRP may increase the effectiveness of the treatment in comparison to patients who have not observed the preparatory steps.

NCT ID: NCT04111068 Completed - Clinical trials for Macular Degeneration

Improving Vision in Adults With Macular Degeneration

Start date: December 1, 2019
Phase: N/A
Study type: Interventional

The purpose of this study is to test whether a kind of brain stimulation called anodal transcranial direct current stimulation (a-tDCS) can improve the ability of people with age-related macular degeneration (AMD) or juvenile macular degeneration (JMD) to read words presented to them on a computer screen. In addition, secondary measures of visual acuity will also be examined to determine whether brain stimulation can allow patients to resolve finer details of an image. The proposed treatment is the application of a-tDCS onto the participant's head, with brain stimulation aimed at Primary Visual Cortex toward the occipital pole. The investigators will test the ability of participants to read words before and after the application of stimulation. The difference between the pre and post tests when receiving active stimulation will be compared to the difference when receiving sham stimulation, because sham stimulation is not expected to improve reading beyond a placebo. The aim of the study is to examine the potential of brain stimulation as an effective treatment for macular degeneration that may be used in conjunction with more traditional eye-based interventions. The investigators hypothesize that the brain stimulation will enable higher performance in the reading task and secondary measures due to an increase in the cortical excitability of the stimulated brain cells.