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NCT ID: NCT02389257 Terminated - Healthy Clinical Trials

Optically Pumped 4He Magnetometers Performances Compared With Medical Reference Methods (ECG and MEG)

MINIMAG
Start date: January 2015
Phase: Phase 1
Study type: Interventional

Optically Pumped 4He Magnetometers operability for cerebral and cardiac magnetic fields measurement.

NCT ID: NCT02388165 Terminated - Clinical trials for Staphylococcal Vaccine

Safety and Efficacy of SA4Ag Vaccine in Adults Having Elective Open Posterior Spinal Fusion Procedures With Multilevel Instrumentation

STRIVE
Start date: July 2, 2015
Phase: Phase 2
Study type: Interventional

The purposes of the clinical trial are to determine whether the SA4Ag vaccine can prevent postoperative Staphylococcus aureus infections in patients who are undergoing elective spinal fusion surgery, and to evaluate the safety of SA4Ag in patients who are undergoing elective spinal surgery.

NCT ID: NCT02387216 Terminated - Clinical trials for Non-Small Cell Lung Cancer

A Study of MM-121 in Combination With Chemotherapy Versus Chemotherapy Alone in Heregulin Positive NSCLC

SHERLOC
Start date: February 1, 2015
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether the combination of MM-121 plus docetaxel is more effective than docetaxel alone in regards to PFS in patients with heregulin-positive NSCLC.

NCT ID: NCT02385903 Terminated - Clinical trials for Necrotic Arterial Wounds

Randomized Controlled Trial on the Use of Flammacerium in Necrotic Arterial Wounds of the Lower Limb Versus Standard Treatment

Flammacérium
Start date: September 2009
Phase: Phase 2
Study type: Interventional

Ischemia of an area may lead to a necrotic wound. In lower limb, it especially happens in diabetic or artheriopatic patients. It can lead to an amputation need. Revascularization procedure cannot be provide in all cases. Flammacerium, by a crust training and its anti-inflammatory effect, could stabilize necrosis extension, avoid bacterial contamination and then improve some incapacitating symptoms like odor or pain. This product may allow to delay amputation ruling for patients on who this procedure is unsafe. During 6 months, the investigators evaluate Flammacerium against standard dressing procedure in necrotic wound of the lower limb in patients where no revascularization can be provide. The investigators observed its effect on amputation need, symptoms as pain, infection, wound aspect evolution, wound size decrease.

NCT ID: NCT02383095 Terminated - Schizophrenia Clinical Trials

Efficiency of Art-therapy in Psychotic Disorders

Start date: May 27, 2015
Phase: N/A
Study type: Interventional

The main purpose of the protocol is to test the efficiency of art-therapy versus metacognitive rehabilitation on the visual perception disorders observed in patients with schizophrenia.

NCT ID: NCT02381756 Terminated - Clinical trials for Dysfunction, Left Ventricular

Ultrasound and Left Ventricular Systolic Function

EFESE
Start date: November 2015
Phase:
Study type: Observational

The aim of this study is to evaluate, in an intensive care unit, the reproducibility between two non-cardiologists operators and a cardiologist expert in echocardiogram, of the Simpson method and of the calculation of GLS for the evaluation of the systolic function of the left ventricle in critically ill patients intubated and ventilated.

NCT ID: NCT02378779 Terminated - Clinical trials for Premature Ejaculation

Consultations Reason for Genital, Urinary or Psychological Humans in General Practice

GETUP
Start date: April 22, 2016
Phase: N/A
Study type: Interventional

Many male patients complain about their ejaculation: 21-30% of men aged between 18 and 59 have admitted suffering from a decrease in, or loss of control of, their ejaculation. The quality of life of patients and their partners is impaired compared to men not suffering from premature ejaculation. Economically, the impact of the disease are significant. In the year preceding the detection of premature ejaculation patients visit twice their physician. The majority of men interviewed anonymously, in their General Practitioner's ( GP's) waiting room, considered it important to talk with their GP about their sexual concerns. Almost half of them preferred that their GP initiate any discussions about sexuality. More than two thirds of the respondents would have liked their GP to signal his or her open-mindedness by directly addressing sexual topics during the consultation. In 2008 a qualitative study brought to the fore the strategies used by GPs to initiate the discussion on premature ejaculation . GPs who mentioned premature ejaculation with their patient described three attitude-related strategies and three investigative strategies.

NCT ID: NCT02377609 Terminated - Validation Clinical Trials

To Validate an Analytical Method to Measure Concentration of Tacrolimus in Blood Taken From Finger Pricks

Start date: October 2013
Phase: N/A
Study type: Observational

The principal aim of this study is to define the relationship between tacrolimus concentrations determined from the finger prick DBS (Dry Blood Spot) method and those determined from blood samples collected by venepuncture in transplant recipients.

NCT ID: NCT02377518 Terminated - Clinical trials for For Oncologic Patients

DECT Ventilation Imaging

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

Demonstrate the feasibility of dual energy computed tomography using Krypton as a gaseous contrast media in order to study the in vivo ventilation. Two different clinical situations will be tested : - Prediction of postoperative pulmonary function for oncologic patients - Detection of Bronchiolitis Obliterans in lung transplant recipients.

NCT ID: NCT02377219 Terminated - Clinical trials for Female Reproductive Problem

Bisphenol A Exposure, Ovarian Function and Assisted Reproductive Technology Outcome.

FIVPHENOL
Start date: October 2014
Phase: N/A
Study type: Interventional

Our goal is to prospect the relationships between Bisphenol A (BPA) exposure (measured as its free and conjugated forms in blood and urine) and embryo implantation rate (measured as the ratio between the number of gestational sacs and the number of transferred embryos) after assisted reproductive technology. In order to reduce the confusion factors, the population study is limited to young women (aged 28 to 34), with regular menstrual cycles and without any medical event that could affect the implantation process