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  • InvestigatioN of a Smart Probe for Lung lEsion Characterization Using Impedance Technology

    Participants in this study require a lung biopsy to confirm if they have a lung tumour. A biopsy is a procedure where a piece of lung tissue is removed for testing. Current biopsy techniques cannot guarantee the exact location of lung tumours, so biopsies can be taken from healthy tissue. The BioSpy System (BSS) is a device with a probe, which is placed inside a normal biopsy needle. The tip of the probe contains sensors, that will scan the composition of the tissue which is in contact with the sensors. The INSPECT study aims at collecting the sensor data, with the goal of being able to differentiate the different tissues. All study participants will have a biopsy with the BSS. Participants will have a hospital visit for the procedure, and will have to stay up to 16 hours after their procedure as per normal hospital practice.

    Phase

    N/A

    Span

    53 weeks

    Sponsor

    Sensome

    Le Plessis-Robinson

    Recruiting

  • Zenith Thoracic Alpha (ZTA) Post-Market Data Collection

    Per local regulations, this study includes both retrospective and prospective patients. Patients can be included retrospectively if they are treated with the study device from 01 January 2019 until the study site is eligible for prospective enrollment.

    Phase

    N/A

    Span

    587 weeks

    Sponsor

    Cook Research Incorporated

    Le Plessis-Robinson

    Recruiting

  • European Aortic Data Collection Project

    Phase

    N/A

    Span

    396 weeks

    Sponsor

    Cook Research Incorporated

    Le Plessis-Robinson

    Recruiting

  • Immunologic Risk of Pregnancy in Women With Lung Transplantion : a National Multicentric Study

    Phase

    N/A

    Span

    57 weeks

    Sponsor

    Nantes University Hospital

    Le Plessis-Robinson

    Recruiting

    Healthy Volunteers

  • Prevention Atrial Fibrillation by BOTulinum Toxin Injections (BOTAF)

    Botulinium toxin use has been developed with success in wide-ranging fields (neurology, otorhinolaryngology, gynaecology, urology, plastic surgery, pain therapy), but not in cardiology. In the cardio-vascular field, only one pilot study on man has shown its utility in the prevention of atrial fibrillation by blocking the triggering through the sympathic and parasympathic systems. The investigators need to assess its potential benefits to prevent postoperative atrial tachyarrhythmia in a randomised multicentre study, with an expected impact of approximately 30,000 patients per years in France undergoing these types of cardiac surgery. The investigators hypothesize that botulinum toxin injection may substantially reduce postoperative AF during the first 3 weeks after cardiac surgery without any serious adverse events. By the suppression of ganglionic plexi (GP) activity in the epicardial fat pads, mild term antiarrhythmic effects can be achieved with fewer antiarrhythmic drugs and anticoagulant treatment.

    Phase

    3

    Span

    366 weeks

    Sponsor

    Assistance Publique - Hôpitaux de Paris

    Le Plessis-Robinson

    Recruiting

  • Extracorporeal Membrane Oxygenation (ECMO) and Coronavirus Disease (COVID) 19

    The main objective of this study is to evaluate the hospital survival of COVID-19 patients supported by venovenous or venoarterial ECMO in a multicenter registry. The secondary objectives are to describe the characteristics of COVID-19 patients who have received ECMO support, to identify the risk factors associated with hospital mortality, to analyze the outcomes after ECMO weaning including survival at day 28 and day 90, and to analyze the utility of a circulatory support mobile unit in a severe pandemic Inclusions are both prospective and retrospective in order to collect data over the whole pandemic

    Phase

    N/A

    Span

    27 weeks

    Sponsor

    Rennes University Hospital

    Le Plessis-Robinson

    Recruiting

  • Hypnosis Versus SIVOC by Remifentanil During TAVI Procedures : Iloact on Peripoperative Confusion

    Each included patient will randomly be assigned either to the hypnosis group or to the remifentanil group. Patients of the hypnosis group will have one preoperative and one perioperative hypnosis session with a qualified anesthesiologist. Patients of the remifentanil group will receive sedation with remifentanil, administered using a pre specified target controlled-infusion protocol. Incidence of delirium will be recorded in the cardiac intensive care unit (CICU) during the first 72 postoperative hours, using the Confusion Assessment Method in the ICU (CAM-ICU). Incidence of other complications such as episodes of oxygen desaturation, vascular wound, stroke, general anesthesia requirement and inhospital death will be recorded, as well as procedure duration, hospital length of stay, patient satisfaction and operator comfort. Transcatheter aortic valve implantation (TAVI) procedures are frequently complicated with postoperative delirium.

    Phase

    N/A

    Span

    157 weeks

    Sponsor

    Centre Chirurgical Marie Lannelongue

    Le Plessis-Robinson

    Recruiting

  • Evaluation of Diaphragmatic Function After Bi-pulmonary Transplantation

    Phase

    N/A

    Span

    105 weeks

    Sponsor

    Centre Chirurgical Marie Lannelongue

    Le Plessis-Robinson

    Recruiting

  • Lung Transplantation for Pleuroparenchymal Fibroelastosis

    Phase

    N/A

    Span

    31 weeks

    Sponsor

    Hospices Civils de Lyon

    Le Plessis-Robinson

    Recruiting

  • A Study of TAK-330 to Reverse the Effects of Factor Xa Inhibitors For Adults Needing Urgent Surgery

    Phase

    3

    Span

    294 weeks

    Sponsor

    Takeda

    Le Plessis-Robinson

    Recruiting

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