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NCT ID: NCT01803893 Enrolling by invitation - Pregnancy Clinical Trials

Prognostic Value of PIF Detection in Embryo Culture Media Correlation With Pregnancy Outcome

PIF-SET1
Start date: September 2012
Phase: N/A
Study type: Observational

PIF: biomarker of successful implantation To overcome the poor reproductive potential of embryos generated during in vitro fertilization cycles and the lack of markers enabling the identification of the most competent ones, it is common to transfer multiple embryos. However this practice is associated with the risks of multi-fetal pregnancies and high morbidity/mortality. Ideally, the availability of a marker specifically produced by viable embryos would permit the transfer of a single embryo (SET) without affecting the chances of pregnancy and, most importantly, capable to drastically reduce multiple pregnancies after IVF. In preliminary work, we demonstrated that no pregnancy resulted following the transfer of embryos where PIF was undetectable in culture media.(Keramitsoglou, T et al. ASRI Meeting, Hamburg, 2012) Using a non-invasive method of detection of PIF in the media surrounding the embryo will be correlated to live birth following single embryo transfer. By selecting only viable embryos, it will reduce the need for multiple IVF cycles, increase the rate of pregnancy outcome associated with SET, and will minimize multi-fetal pregnancy that has very high medical and societal costs both in pregnancy and after delivery.

NCT ID: NCT01715402 Enrolling by invitation - Clinical trials for Hepatocellular Carcinoma

Optimization of Health Expenditure in Liver Surgery

Start date: September 2012
Phase: N/A
Study type: Observational

The aim of this study is to reduce the length of stay after liver surgery by taking account of objective quantitative clinical variables, subjective qualitative clinical variables and non clinical variables.

NCT ID: NCT01708005 Enrolling by invitation - Clinical trials for Mild Cognitive Impairment

DIetary Supplements, Executive funcTions and Vitamin D (DIET-D)

DIET-D
Start date: November 2012
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study is to compare the effect after 12 weeks of the oral intake of Lecitone®Se + 200UI/day of D3 vitamin with the effect of a placebo on changes in cognitive performance in Trial Making Test score part B (this test evaluate executive functions of mental flexibility) in older adults with Mild Cognitive Impairment (MCI).

NCT ID: NCT01687647 Enrolling by invitation - Lung Neoplasms Clinical Trials

Sputum Cytometry Analysis in Lung Cancer Screening After Professional Asbestos Exposure

AMORCE-CBP
Start date: September 2012
Phase: Phase 3
Study type: Interventional

Workers exposed to asbestos are at high risk of lung cancer. Medical follow-up of this population relies on repeated CT-scans which are more accurate for detection of peripheral lesions, and expose to X-rays and to risk of false-positives. Analysis of sputum using automate cytometry may be of interest in this population, alone or in combination with CT-scan. An ancillary study will evaluate the interest of blood predictive biomarkers.

NCT ID: NCT01569217 Enrolling by invitation - Respiratory Failure Clinical Trials

Regional Distribution of Ventilation to Assess Respiratory Muscle Dysfunction

DREM
Start date: June 2011
Phase: N/A
Study type: Observational

The aim of this study is to better discriminate respiratory muscle dysfunction by comparing the measurements of thoracoabdominal motion obtained by an optoelectronic recording and the conventional tests of respiratory muscle strength. The final objective is to better select in the future the patients who need more specific assessment of diaphragmatic function like "maximal transdiaphragmatic pressure" measurement and "phrenic nerve stimulation".

NCT ID: NCT01333345 Enrolling by invitation - Cataract Clinical Trials

Post-Implant Performance of the EC-3 IOL

Start date: April 2011
Phase: N/A
Study type: Observational

The purpose of this study is to obtain data on the performance of the EC-3 lens at an interval of two years (and beyond) from subjects who were implanted. The primary aim of the study will be to evaluate the presence, if any, of PCO, lens glistening, and other anomalies in the subjects.

NCT ID: NCT00904774 Enrolling by invitation - Clinical trials for Bronchopulmonary Dysplasia

Genetic Susceptibility for Bronchopulmonary Dysplasia in Preterm Infants

GENBPD
Start date: May 2009
Phase: N/A
Study type: Observational

Despite considerable obstetric and neonatal advances in the care of very low birth weight (VLBW) neonates, bronchopulmonary dysplasia (BPD) continues to occur among 20 to 40% of surviving infants, and new ways for combatting this disease must be found. BPD appears to result from arrested lung development, but its etiology has not yet been fully established. Besides the role of the exposure of the immature lung to injurious factors in the development of BPD, a genetic susceptibility for BPD in preterm infants was recently evidenced. Taking advantage of new genomic technologies, the objective of the investigators' project is to identify predisposing human genetic variants through: 1. a genome-wide association (GWA) study in VLBW neonates, 2. a candidate-gene association study, including selection of single nucleotide polymorphisms (SNPs) found in (a) and 3. functional studies of any SNP found to be convincingly associated with BPD in (a) and (b).

NCT ID: NCT00848198 Enrolling by invitation - Dry Eye Disease Clinical Trials

TearLab Core Validation Study

CVS
Start date: February 2009
Phase: N/A
Study type: Observational

This is a global study of tear osmolarity using the OcuSense TearLab technology to compare tear samples of age and sex-matched normals with those with Dry Eye Disease (DED). Diagnosis of DED subjects will be established using objective and subjective tests. Positive responses to 3 out of 6 defined criteria determine subjects with DED. DED subjects will be further categorized by severity, using results from the objective and subjective tests. Subjects will be assessed at a single visit.

NCT ID: NCT00770627 Enrolling by invitation - Clinical trials for Attention Deficit Hyperactivity Disorder

Clinical Trial to Evaluate the Efficacy and the Tolerance of an Omega 3 Fatty Acids Supplementation in ADHD Children

Start date: October 2008
Phase: Phase 4
Study type: Interventional

Principal focus is to evaluate the effects of omega 3 fatty acids supplementation on the ADHD children's behaviour during 12 weeks on two years. The secondary focus is to evaluate the effects of omega 3 fatty acids supplementation on the lexical level,intentional abilities, anxiety and depression. The omega 3 fatty acids don't present adverse side effects. The inclusion to the trial could avoid the intake the methylphenidate and its associated adverse side effects.

NCT ID: NCT00604110 Enrolling by invitation - Heart Failure Clinical Trials

Biventricular Epicardial Pacing Post Cardiac Surgery in Patients With Left Ventricular Ejection Fractions Less Than 45%

Start date: February 2008
Phase: Phase 3
Study type: Interventional

Patients with reduced left ventricular function are at an increased perioperative risk and often need prolonged postoperative treatment on intensive care units. A significant portion of these patients require postoperative pacing. Right ventricular pacing has been shown to be hemodynamically deleterious The aim of this study is to determine which biventricular pacing after cardiac surgery, in patients with reduced left ventricular function (EF≤ 45%), is hemodynamically favourable.