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NCT ID: NCT02813408 Completed - Prostatic Neoplasms Clinical Trials

A Study to Investigate the Impact of Abiraterone Acetate and Enzalutamide on Health-related Quality of Life, Participant-Reported Outcomes, and Medical Resource Use in Metastatic Castration-resistant Prostate Cancer Participants

AQUARiUS
Start date: May 3, 2016
Phase:
Study type: Observational

The purpose of this observational study of metastatic castration-resistant prostate cancer (mCRPC) participants is to explore whether or not there are differences between participants treated with abiraterone acetate and enzalutamide on the health-related quality of life (HRQoL), Fatigue, Pain, Cognitive function and medical resource use (MRU).

NCT ID: NCT02813317 Completed - Breast Cancer Clinical Trials

Optimizing the Care Pathways of Patients Treated for Operable Breast.

OPTIsoins01
Start date: December 2014
Phase: N/A
Study type: Observational

This prospective, multicenter, observational study aims to explore a comprehensive approach to the care of early breast cancer patients in a regional health territory (including 1.5 million women and characterized by a breast cancer incidence and mortality higher than national ranges), incorporating all healthcare actors inside and outside the hospital.

NCT ID: NCT02813291 Completed - Aging Clinical Trials

MI Practice and tDCS With Aging

MISt
Start date: April 26, 2017
Phase: N/A
Study type: Interventional

The mental repetition of movements - or motor imagery (MI) practice - facilitates motor learning. It allows avoiding fatigue that occurs during physical practice; this method is thus particularly interesting for elderly people. Transcranial direct current stimulation (tDCS) is a noninvasive method of neurostimulation during which a low direct current is applied to the brain via electrodes placed on the scalp. This method has been successfully used to enhance motor learning in both young and elderly subjects. The main aim of this study is to assess the impact of MI practice combined with tDCS on the learning of a complex finger sequence, in young and elderly subjects. For that purpose, young and elderly healthy subjects will be randomly assigned to Stimulation and Sham groups. There will thus be a total of four groups: Young Stim, Young Sham, Elderly Stim, and Elderly Sham. All subjects will participate to three training sessions spread over five days, and a retention test one week after the third training session. During training they will mentally repeat a complex finger sequence with the left hand, for 13 min: - Subjects of the Stimulation groups (Young Stim and Elderly Stim) will receive in parallel an anodal tDCS of the primary motor cortex. - Subjects of the Sham groups (Young Sham and Elderly Sham) will receive in parallel a sham tDCS of the primary motor cortex. Immediately before (pretest) and after (posttest) each training session, as well as during the retention test, subjects will repeat the sequence as many times of possible, for 1 min. During these tests (pretests, posttests and retention test) electroencephalographic activity will be recorded to assess the Mu rhythm power.

NCT ID: NCT02813200 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease (COPD)

Description of the Ability to Learn How to Handle Inhaler Devices in COPD

INTUITIVE
Start date: January 10, 2017
Phase: Phase 4
Study type: Interventional

Chronic Obstructive Pulmonary Disease (COPD) is the fourth leading cause of death in the world and further increase in its prevalence and mortality has been predicted. Currently, the main long-term treatments are the long-acting beta-2 agonist, indacaterol, salmeterol and the anticholinergic drug, tiotropium and glycopyrronium, used alone or in combination: - long-acting beta-2 agonist with corticosteroid (e.g. salmeterol/fluticasone), - long-acting beta-2 agonist with anticholinergic (e.g. indacatetrol/glycopyrronium). These drugs are delivered to the lung using different inhaler devices such as Breezhaler ®, Handihaler® and Diskus®.

NCT ID: NCT02812979 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Evaluation of the Effectiveness of the Nebulization Bronchodilators Under High Nasal Flow Humidified

AirvoNEB
Start date: June 2016
Phase: N/A
Study type: Interventional

The principal objective is to show noninferiority of nebulized salbutamol through the high flow nasal system moistened AIRVO ™ 2 in terms of reversibility of airflow obstruction compared to nebulization by the usual method (spray mask).

NCT ID: NCT02812901 Completed - Myocardial Ischemia Clinical Trials

Tolerance of Myocardium to Ischemia Injury

TOMIS
Start date: January 2016
Phase: N/A
Study type: Interventional

This study aims to understand the impact of time-of-the day on human myocardial tolerance to ischemia-reperfusion by exploring atrial myocardium biopsied during cardiac surgery. Patients scheduled for non-urgent cardiac surgery (coronary artery by-pas graft and/or aortic valve replacement) will be assigned to a morning or an afternoon cardiac surgery based on randomization. Myocardial biopsies will be explored in ex vivo conditions mimicking ischemia-reperfusion.

NCT ID: NCT02812810 Completed - Smoking Cessation Clinical Trials

Evaluation of the Efficacy of Repetitive Transcranial Magnetic Stimulation (rTMS) Low-frequency on Craving in Smoking Dependence

rTMS TABAC
Start date: September 2011
Phase: N/A
Study type: Interventional

The fight against smoking is a public health priority. Without help, fewer than 5% of des smokers are abstinent at 12 months after smoking cessation. Despite well-managed attempts at smoking cessation with nicotine substitutes, the rate of success at 12 months in patients dependent on nicotine is only 18%. Moreover, other therapeutic strategies (acupuncture, hypnosis…) have not proved to be effective. The investigators propose a new therapeutic strategy for smoking cessation, which is based on associating nicotine substitutes (to reduce physical symptoms of weaning from nicotine) with rTMS at 1 Hz to the right DorsoLateral PreFrontal Cortex (DLPFC) for 2 weeks (to diminish craving for tobacco). The principal objective is to improve the success rate for smoking cessation attempts in patients who are highly dependent on nicotine, and who have failed using usual smoking cessation strategies.

NCT ID: NCT02812758 Completed - Thoracic Surgery Clinical Trials

Does Sedation Depth (as Evaluated by the Bispectral Index) Influence Dynamic Indices of Preload Dependence?

BIS2
Start date: December 2015
Phase:
Study type: Observational

Dynamic indices of preload dependence (such as stroke volume variability -SVV , pulse pressure variability - PPV and plethysmograph variability index - PVI ) are reportedly predictive of the response to vascular filling in sedated, mechanically ventilated patients. However, the influence of the sedation depth on these dynamic indices has never been evaluated.

NCT ID: NCT02812745 Completed - Thoracic Surgery Clinical Trials

Is the Decrease in the Bispectral Index Correlated With a Decrease in Cardiac Output During the Induction of Anaesthesia?

BIS1
Start date: October 2015
Phase:
Study type: Observational

Monitoring the bispectral index (BIS) as a peri-operative hemodynamic tool appears to be justified by the agreement between various clinical situations in which BIS monitoring appears to be of value: the prognosis in traumatic head injury, the diagnosis of brain death , and the diagnosis of amniotic fluid embolism. The current controversy concerning the "triple low" state reinforces the need for an accurate study in this field. Furthermore, the recent review by Bidd argues in this sense.

NCT ID: NCT02812563 Completed - Keratoconus Clinical Trials

Familial Analysis of Keratoconus Risk

AFRIK
Start date: November 25, 2014
Phase: N/A
Study type: Observational

The principal objective of this study is to evaluate the frequency of KC inside family of patients with confirmed KC. It's a familial, epidemiological, prospective, single-center study.