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NCT ID: NCT02594124 Completed - Clinical trials for Spinal Muscular Atrophy

A Study for Participants With Spinal Muscular Atrophy (SMA) Who Previously Participated in Nusinersen (ISIS 396443) Investigational Studies

SHINE
Start date: November 4, 2015
Phase: Phase 3
Study type: Interventional

The primary objective is to evaluate the long-term safety and tolerability of nusinersen (ISIS 396443) administered by intrathecal (IT) injection to participants with Spinal Muscular Atrophy (SMA) who previously participated in investigational studies of nusinersen. The secondary objective is to examine the long-term efficacy of nusinersen administered by IT injection to participants with SMA who previously participated in investigational studies of nusinersen.

NCT ID: NCT02594059 Completed - Pulmonary Fibrosis Clinical Trials

Assessment of Peripheral Endothelial Function in Idiopathic Pulmonary Fibrosis

Endoth-FPI
Start date: December 19, 2012
Phase: N/A
Study type: Interventional

The aim of the study is to assess the peripheral endothelial function in adult patients with idiopathic pulmonary fibrosis (IPF) and the relationship between the peripheral endothelial function and the severity of the IPF.

NCT ID: NCT02594020 Completed - Dental Caries Clinical Trials

Comparison of Different Methods of Enamel Preparation Before Pit and Fissure Sealants

Start date: June 2008
Phase: N/A
Study type: Interventional

This study concerns the prevention of dental caries by sealing pits and fissures of permanent molars with a photopolymerizable resin. It must compare these three techniques Microdentisty (air abrasion, abrasion and sound using small cutters) usually used to prepare micro cavities in the enamel and / or the outer third of the dentin. These three commonly used techniques have never been compared by retaining as endpoint retention of sealant. These techniques are painless and do not require local anesthesia.

NCT ID: NCT02593461 Completed - Infertility Clinical Trials

Diafert® for Embryo Selection and Fertility Improvement

DESTINy
Start date: October 22, 2015
Phase: Phase 3
Study type: Interventional

Prospective, single-center, single-blind, randomized, controlled, two-arm, interventional study.

NCT ID: NCT02593357 Completed - Clinical trials for Chronic Obstructive Pulmonary Disease

Peripheral Endothelial Function in COPD Patients

endothBPCO
Start date: December 17, 2012
Phase: N/A
Study type: Interventional

The aim of the study is to assess the peripheral endothelial function in adult COPD (chronic obstructive pulmonary disease) patients and the relationship between the peripheral endothelial function and the pulmonary function.

NCT ID: NCT02593344 Completed - Clinical trials for Endothelial Function

Peripheral Endothelial Function in Asthmatic Patients

Endothasthm
Start date: December 13, 2012
Phase: N/A
Study type: Interventional

The aim of the study is to assess the peripheral endothelial function in adult asthmatic patients and the relationship between the peripheral endothelial function and the pulmonary function.

NCT ID: NCT02593292 Completed - Pregnancy Clinical Trials

Program of Research for the Optimization of a Supervised Patient Pathway for Expectant According to Risk in Obstetrics

PROSPERO
Start date: December 5, 2016
Phase: N/A
Study type: Interventional

This French multicentre open-label randomized trial will test the hypothesis that a coordinated health circuit based on obstetric risks, backed up by an electronic patient care reporting information system will optimize the continuum of pregnancy care monitoring. The electronic patient care reporting information system will be shared between patients, private practice physicians/midwifes, hospital physicians/midwifes and supervised by a coordinating midwife.

NCT ID: NCT02593045 Completed - Clinical trials for Cutaneous T-Cell Lymphoma

Study of IPH4102 in Patients With Relapsed/Refractory Cutaneous T-cell Lymphomas (CTCL)

Start date: October 2015
Phase: Phase 1
Study type: Interventional

The primary objective of this first in human study is to assess the safety and tolerability of increasing intravenous (IV) doses of single agent IPH4102 administered to patients with relapsed/refractory CTCL to characterize the dose limiting toxicities (DLT) and identify a Maximum Tolerated Dose (MTD).

NCT ID: NCT02592460 Completed - Postoperative Pain Clinical Trials

Postoperative Pain and Polyamines-poor Diet (DOLAMINE)

DOLAMINE
Start date: December 2014
Phase: N/A
Study type: Interventional

Animal studies have shown that the level of pain sensitivity is highly dependent on the amount of polyamines in food. This fundamental observation of a nutritional approach to pain led the authors to develop diets completely depleted in polyamines whose anti-nociceptive properties have been confirmed in animals. Postoperative pain after foot surgery are currently fairly well controlled but at the cost of a high consumption of grade II analgesics which is associated with a high rate of side effects (nausea, vomiting ...). The investigators' hypothesis is that a diet low in polyamines may have an additive effect on pain control and reduce the consumption of level 2 analgesics. The objective of this study is to show the efficacy of a polyamines-poor diet on postoperative pain in ambulatory surgery of the foot.

NCT ID: NCT02592369 Completed - Clinical trials for Aortic Valve Stenosis

CoreValve™ Evolut R™ FORWARD Study

FORWARD
Start date: January 2016
Phase:
Study type: Observational

Prospective, single arm, multi-center, observational, post market study to document the clinical and device performance outcomes of the Evolut R system used in routine hospital practice in a large patient cohort for the treatment of symptomatic native aortic valve stenosis or a stenosed, insufficient, or combined surgical bioprosthetic valve failure necessitating valve replacement.