Clinical Trials Logo

Filter by:
NCT ID: NCT02818738 Completed - Clinical trials for First Manifestation of Steroid Sensitive Nephrotic Syndrome

Efficiency of Levamisole for Maintaining Remission After the First Flare of Steroid Sensitive Nephrotic Syndrome in Children

NEPHROVIR3
Start date: September 6, 2017
Phase: Phase 3
Study type: Interventional

Idiopathic Nephrotic Syndrome is sensitive to steroid in 90% of children. However, most patients relapse and become steroid-dependant, with a long lasting relapsing course. The aim of this study is to assess the efficiency of a 6-months levamisole course, given early after first remission, on maintaining a relapse-free course at 12 months.

NCT ID: NCT02818725 Completed - KRAS Gene Mutation Clinical Trials

I-MVAC +/- Panitumumab as First-line Treatment of Advanced Urothelial Carcinoma Without H-Ras Nor K-Ras Mutations

GETUG-AFU19
Start date: June 2010
Phase: Phase 3
Study type: Interventional

OBJECTIVES OF THE TRIAL Primary objective Evaluation of efficacy in terms of progression-free survival at 9 months of the combination of intensified methotrexate, vinblastine, doxorubicin and cisplatin with or without panitumumab as first-line treatment of advanced urothelial carcinoma in patients without Harvey nor Kirsten rat sarcoma viral oncogene homolog mutations. Secondary objectives - To assess toxicity - To assess response rate - To assess overall survival - To assess time to progression - To study the correlation between response rate, time to progression, overall survival and biological parameters

NCT ID: NCT02818595 Completed - Infant, Premature Clinical Trials

Development of Maternal Voice Recognition in Preterm Neonates

PREMAVOIX
Start date: March 2013
Phase: N/A
Study type: Interventional

Many cognitive functions in humans are based on asymmetrical brain networks. For example, in most adults, the language is essentially processed by the left hemisphere, while other auditory functions, such as voice recognition, tend to be processed by the right hemisphere. Many studies, especially those conducted by Ghislaine Dehaene's team, have demonstrated the presence of anatomical and functional asymmetries by the first months of life. What are the causes of these asymmetries? How do they develop? Are they necessary for functioning or effective learning? This study, conducted in collaboration with the Compiègne applied mathematics team (Abdelatif El Badia) and the INSERM team (Ghislaine Dehaene), is designed to determine the stage of development at which hemispheric dominance for voice recognition is first observed and to identify the brain structure involved in preterm neonates whose sound environment is usually very different from that of the foetus. The impact of this environment on the infant's brain development and early learning will be evaluated.

NCT ID: NCT02818504 Completed - Clinical trials for Cardiovascular Risk Factor

SEMEiotic Oriented Technology for Individual's CardiOmetabolic Risk Self- assessmeNt and Self-monitoring

SEMEOTICONS
Start date: July 2016
Phase: N/A
Study type: Interventional

Cardio-metabolic risk factors include obesity, physical inactivity, smoke, alcohol abuse, high blood lipids or sugar and arterial hypertension. Systems for self-learning and self-monitoring may help people improve and maintain a healthy lifestyle through tailored suggestions about diet, weight control, physical activity, fatigue,stress. SEMEOTICONS exploits the human face as an indicator of individual's health status and translates signs obtained from the face using contactless sensors into measures and descriptors to be automatically evaluated by a an interactive smart mirror. This "Wize Mirror" extracts descriptors from videos, images and gas concentration signals and integrates them in a virtual model used to compute and trace the evolution of an individual's wellness index. A health diary enables each individual to evaluate and personally relate his/her lifestyle to his/her well-being. Coaching messages are provided, in relation to the evolution of the wellness index and of each descriptor, to provide useful suggestions on correct lifestyle self-monitoring. The purpose of this study is assess the accuracy of the information derived from the Wize Mirror in expressing the health status of the individual. The reproducibility and repeatability study will evaluate whether measurements are stable over short time spans and whether they are influenced by meals light and temperature conditions. To verify whether the Wize Mirror is able to detect variations in physical and emotional health status with appropriate lifestyle changes, the validation study will cross-check measurements from the Wize Mirror against reference clinical tests at enrolment and after 3 months of personalized suggestions for healthy behavior. Reference tests include - Physician visit - Measurement of blood oxygen content and skin end products of sugar metabolism,body composition, energy expenditure, vascular function - Laboratory profile and exhaled gas composition - Questionnaires on quality of life and lifestyle (food, sleep, physical activity, smoking, alcohol, stress). Wize Mirror measures include - 3D reconstruction of face images for roundness, color, stress and fatigue - Heart and respiratory rate - Detection of skin sugar metabolism end-products and of eye lipid deposits - Small vessel vasodilating ability with local heating The results will allow to assess whether the Wize Mirror is easy to use and helpful for self-monitoring of cardio-metabolic risk.

NCT ID: NCT02818465 Completed - Clinical trials for Hemodialyzed Patients

Role of the Interaction Between Advanced Glycation End Products and Their Receptor RAGE in the Development and the Progression of the Uremic Vasculopathy of Hemodialyzed Patients

RAGE-VASCU
Start date: March 30, 2015
Phase: N/A
Study type: Interventional

Chronic kidney disease (CKD) is associated with an extensive vasculopathy and high cardiovascular mortality as well as an accumulation of uremic toxins. Among the latest, advanced glycation end-products (AGEs) interact with RAGE. Investigators aimed to analyze the role of RAGE in the calcification process of hemodialyzed patients, in a correlative and prospective study. Vascular calcifications will be assessed by Xray and tomodentimetry while accumulation of AGEs will be measured in the serum and in the skin (non invasive). Additionally factors influencing RAGE activation such as genetic polymorphism and level of soluble forms of RAGE will be measured and analyzed.

NCT ID: NCT02818374 Completed - Mental Handicap Clinical Trials

The Oral Accessibility Spatula (Spatule SAB)

SAB
Start date: March 2016
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the efficiency and the safe use of a new medical device to improve the oral accessibility of disabled people during the oral-dental examination.

NCT ID: NCT02818231 Completed - Clinical trials for Ethmoid Sinus Adenocarcinoma

Mechanisms of Cancerogenesis of Woodworkers Adenocarcinomas

ADK-FO
Start date: June 2016
Phase: N/A
Study type: Observational [Patient Registry]

Nasal adenocarcinomas are closely related to wood dust exposure. The precise mechanisms of carcinogenesis leading to the transformation of the respiratory mucosa into a colonic-like mucosa remain unknown: chronic exposure to wood dust may cause chronic inflammation that may lead to pre-degenerative lesions, hypothesis yet unconfirmed. The tumor development requires the activation of a particular gene: CDX2. The working hypothesis is that chronic wood dust exposure is responsible for changes in genes of inflammation, which can in turn lead to changes in the expression of CDX2 and its cofactors, thus making possible the genesis of adenocarcinoma. This work is a pilot study aiming to better understand the mechanisms of carcinogenesis, and to study the feasibility of a larger prospective screening for woodworkers adenocarcinomas. Cells will be obtained from the at risk area (olfactory cleft) by a noninvasive method (brushing) in healthy volunteers (unexposed to wood dust) and in exposed volunteers to compare their genomes and study the genomic changes related to wood dust exposure.

NCT ID: NCT02818101 Completed - Clinical trials for Coronary Angiography

Hypnosis Efficacy for the Prevention of Anxiety During a Coronary Angiography

HypCor
Start date: March 2016
Phase: N/A
Study type: Interventional

The purpose of this study is to confirm the utility for hypnosis in the coronary angiographic examination. The technique would be an alternative to prevent the consumption of anesthesic drugs.

NCT ID: NCT02818062 Completed - Endophthalmitis Clinical Trials

Severe Intraocular Infection

Start date: January 2008
Phase: N/A
Study type: Observational

The host-immune reaction to infection is essential for the comprehension of the disease and the development of new therapies. The aim of the study is to describe intraocular cytokines network in aqueous humor using multiplex immunoassay, during severe intraocular infection.

NCT ID: NCT02817880 Completed - Algoneurodystrophy Clinical Trials

Comparison of the Analgesic Effect Between the Motor Cortex Stimulation and the Trans-spinal Stimulation in the Algoneurodystrophy.

ALGOSTIM
Start date: July 25, 2016
Phase: N/A
Study type: Interventional

The purpose of this study is to compare the analgesic effectiveness of two motor cortex neurostimulations (tDCS and rTMS) and the trans-spinal neurostimulation (tsDCS ) in the algoneurodystrophy.