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NCT ID: NCT03357861 Completed - Cancer Clinical Trials

Cancer Patients Treated With Immunotherapy in Intensive Care Unit

IMMUNO-REA
Start date: September 1, 2018
Phase:
Study type: Observational

This work aims to describe the characteristics and methods of management of patients suffering from a solid tumor treated with immunotherapy admitted to intensive care.

NCT ID: NCT03357367 Completed - Clinical trials for Peripheral Arterial Disease

TiVi Evaluation of Microcirculatory Reactivity of the Skin to Galvanic Stimulation: Effect of Aspirin

PIRAAT
Start date: February 8, 2018
Phase: N/A
Study type: Interventional

Prospective interventional study. The aim is to analyze the effect of usual ongoing treatments over microvascular cutaneous response to galvanic current applications (CIV: current induced vasodilatation) with tissue vitality (TiVi) system on the forearm of subjects referred for ultrasound investigations due to suspicion of peripheral disease. Hypothesis is that the use of aspirin (even at low dose) abolishes the response. This test could make it possible to detect the functional effects of low dose aspirin without using biological tests. A routine clinical application could be to use this CIV to verify adherence to aspirin.

NCT ID: NCT03357302 Completed - Clinical trials for Disability or Chronic Disease Leading to Disablement

Risk Factors Associated With the Global Burden of Disease in Reunion Island and Comparison With Mainland France and Indian Ocean Countries

AVIRON-2
Start date: December 1, 2017
Phase:
Study type: Observational

The question posed by this project is that of the regional estimate of the relative importance of the risk factors of the main pathologies. Our hypothesis is that these risk factors are of different relative importance in Reunion Island compared to metropolitan France.

NCT ID: NCT03357198 Completed - Clinical trials for Respiratory Insufficiency

Correlation of Two Methods for Cough Peak Flow Measurement in Intubated Patients

COUGH-ICU
Start date: December 8, 2017
Phase:
Study type: Observational

Cough Peak Flow (CPF) seems to be an efficient tool to assess cough capacity for the intensive care unit (ICU) ventilated patient. CPF can be used in the ventilator weaning process, as reflecting the upper airways protection capacity. CPF requires disconnection of the patient from the ICU ventilator, supplemental material (handheld spirometer, antibacterial filter) and an excellent synchronization between the specialized caregiver and the patient. We aimed that CPF with the ventilator built-in flow-meter is correlated with CPF using a handheld flowmeter connected to the endotracheal tube.

NCT ID: NCT03357107 Completed - Clinical trials for Supraglottic Squamous Cell Carcinoma

Local Control After Robot-assisted Supraglottic Laryngectomy

Start date: October 1, 2016
Phase: N/A
Study type: Observational

Transoral robotic surgery is an option to treat supraglottic squamous cell carcinomas. Oncological outcomes 2 years after transoral robotic surgery for supraglottic laryngectomy were studied.

NCT ID: NCT03357016 Completed - Overweight Clinical Trials

HIIT Versus MICT on Abdominal Fat Mass and Lipid Oxidation in Postmenopausal Women (MATISSE)

MATISSE
Start date: February 1, 2017
Phase: N/A
Study type: Interventional

Postmenopausal women, as men, are more prone to central or android obesity than premenopausal women. Abdominal fat mass accumulation is associated with an increase of cardiovascular disease (CVD) risk. Most exercise programs designed for weight loss have focused on about 30 min several times per week of moderate intensity continuous training (MICT). Disappointingly, such exercise programs have led to either none or low fat loss. Accumulating evidence suggests that high intensity interval training (HIIT) should be an effective exercise protocol for reducing body fat of overweight individuals, especially at the abdominal level. Resistance Training (RT) is associated with increased muscle mass and strength gain in main muscles groups. Thus, RT seems to be an interesting strategy to fight against deconditioning and autonomy loss with age. Development of muscle mass enhances resting metabolism rate. Thus, RT could raise daily energy expenditure ie. substrates' oxidation including lipids. The aim of our study was to compare the effects of a 12-week moderate intensity continuous training (MICT) program with high intensity interval training (HIIT) program combined or not with a resistance training (RT) program on total abdominal and visceral fat mass and substrate utilization in postmenopausal women. It is hypothesized that HIIT compared to MICT program would result in significantly greater whole body and regional fat mass losses (abdominal and visceral) and would improve lipid oxidation at rest and during prolonged moderate exercise. It is also hypothesized that HIIT associated with RT could be the best strategy to reduce fat mass.

NCT ID: NCT03356847 Completed - Cataract Clinical Trials

Evaluation of the Rotational Stability of the Monofocal SISA Implant Following Cataract Surgery

SISALens
Start date: September 29, 2017
Phase: N/A
Study type: Interventional

A good efficacy as well as good rotary stability is expected with the ocular implant.

NCT ID: NCT03356717 Completed - Simulation Clinical Trials

Effect of an Observer Tool on Learning Outcomes During High Fidelity Simulation

Start date: June 23, 2017
Phase: N/A
Study type: Interventional

The increasing use of high-fidelity simulation is limited by the imbalance between the growing number of students and the human resources available in such a way that all residents cannot play a role during scenarios. The learning outcomes of observers need to be studied in more depth. Previous studies have provided controversial results but overall no significant differences in learning outcomes can be demonstrated between observers and participants engaged as players in scenarios. Moreover, preliminary data suggest that learning outcomes of observers might be improved by using an observer tool during the scenario. However, no high-quality study has yet shown if this assumption is verified. In the present study, 3rd-4th year residents in anesthesia will be randomized before high fidelity scenarios to act as observers only or active participants in some scenarios and observers in others. The main outcome parameter will be the learning outcomes by comparing data obtained before and after the sessions by using questionnaires specifically dedicated to the knowledge of technical skills in the management of crisis scenarios.

NCT ID: NCT03356548 Completed - Clinical trials for Hemochromatoses, Genetic

Transferrin Saturation and Asthenia in Hemochromatosis

HEMOSAT
Start date: April 10, 2017
Phase:
Study type: Observational

Observational study.

NCT ID: NCT03356522 Completed - Clinical trials for Chronic Renal Failure

Study of Trabecular Bone Score (TBS) as a Fracture Risk Factor in Chronic Renal Failure

TRIFIR
Start date: February 1, 2016
Phase: N/A
Study type: Observational

Observational study