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NCT ID: NCT03965338 Completed - Clinical trials for Functional Magnetic Resonance Imaging

Assessment of Brain Activity During Complex Fine Hand Movements: an fMRI Study

Start date: January 1, 2019
Phase: N/A
Study type: Interventional

Brain cortex controls movement but the influence of peripheral component of movement on the cortex is not known. Functional Magnetic Resonance Imaging(fMRI) studies in stroke and fantom limb patients investigate cortex areas activated during execution and imagination of complex hand movements. These studies aim to understand the mechanisms of the motor component of movement but the results are limited as there is no effector organ in fantom limb patients and the affecting organ is damaged in stroke patients. The investigators hypothesized that the areas of the cortex that is activated to remember, set-up and order to move can be isolated from the areas that are activated during the motor component of movement. To prove this hypothesis the investigators developed a model that investigate the brain activation areas during the patient try to execute and imagine doing a complex motor task (sequential opposition with the thumb to the other four fingers) with a peripherally blocked arm. Brain fMRI in 15 right-handed patients scheduled to undergo right-hand surgery with peripheral block anesthesia will be obtained before the surgery day and just before surgery after the block. Participants will be screened when executing the task (after the block they just attempt), during rest and during they imagine doing the task. Bilateral cortex activation areas will be compared when the right hand was intact and was peripherally blocked. There are many unknowns in the relationship between the brain-peripheric organ during movement. The investigators hope that some of these mechanisms will be identified by the new model we used in our study. The final benefit will be to develop stroke therapies and new therapies for neuropathic pain which is closely related to motor function.

NCT ID: NCT03965078 Completed - Epiretinal Membrane Clinical Trials

Epiretinal Membrane and Cystoid Macular Oedema Post-cataract Surgery

EPIC
Start date: June 21, 2018
Phase:
Study type: Observational

This study examines whether the presence of an epiretinal membrane affects the time to resolution, requirement for non-topical treatment, and outcome of pseudophakic cystoid macular oedema.

NCT ID: NCT03964636 Completed - Clinical trials for Combined Oral Contraceptives Intake

Contraceptive Pills and Retinal Vascularization

PILURET
Start date: July 17, 2019
Phase:
Study type: Observational

The main hypothesis is the taking of combined 1st and 2nd generation or 3rd and 4th generation oral contraceptives is associated with a change in retinal micro-vascularization compared to the absence of combined oral contraceptive intake. Women of childbearing age will be recruited during their ophthalmologic consultation at the Rothschild Foundation, an OCT-A will be realized and data relating to their medical and ophthalmologic history and their oestro-progestative contraceptive intake will be collected. The objective is to find an association between retinal vascular density and combined oral contraceptives intake.

NCT ID: NCT03964493 Completed - Clinical trials for Gram-Positive Bacterial Infections

TNP-2092 to Treat Acute Bacterial Skin and Skin Structure Infection

P2_ABSSSI
Start date: April 20, 2019
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate safety, tolerability, pharmacokinetic characteristics and efficacy of TNP-2092 in adults with ABSSSI suspected or confirmed to be caused by gram-positive pathogens.

NCT ID: NCT03964207 Completed - Clinical trials for Pulmonary Disease, Chronic Obstructive

A Study on Whether Patients Prefer the Spiriva® Respimat® or the Spiriva® Handihaler® for Treating Their Chronic Obstructive Pulmonary Disease (COPD)

Start date: November 25, 2019
Phase: Phase 4
Study type: Interventional

The objective of this study is to investigate the patient acceptability/preference of Respimat® compared with Handihaler® in patients with moderate to very severe chronic obstructive pulmonary disease (COPD) to demonstrate the superiority of Respimat®.

NCT ID: NCT03963947 Completed - Clinical trials for Rhinoconjunctivitis With or Without Allergic Asthma

Study to Assess the Safety and Effectiveness of Beltavac® Polymerized With House Dust Mites

Start date: June 1, 2019
Phase:
Study type: Observational

Non-interventional Study to Assess the Safety and Effectiveness Profile of a SCIT Therapy With Beltavac® Polymerised With House Dust Mite in pediatric allergic patients

NCT ID: NCT03963921 Completed - Clinical trials for NASH - Nonalcoholic Steatohepatitis

Safety and Tolerability of HepaStem in Patients With Cirrhotic and Pre-cirrhotic NASH Patients

PANASH
Start date: April 9, 2019
Phase: Phase 1/Phase 2
Study type: Interventional

Multicenter, open-label, safety and tolerability study of ascending doses of HepaStem in patients with cirrhotic and pre-cirrhotic non-alcoholic steato-hepatitis (NASH) to determine the safety and tolerability of ascending single and repeated doses of HepaStem administered to patients with cirrhotic and pre-cirrhotic non-alcoholic steato-hepatitis (NASH)

NCT ID: NCT03963336 Completed - Clinical trials for Idiopathic Intracranial Hypertension

Quantitative D-dimer Level and Anticoagulant Therapy in Idiopathic Intracranial Hypertension

Start date: July 22, 2017
Phase: Early Phase 1
Study type: Interventional

Idiopathic intracranial hypertension (IIH) is a syndrome characterized by elevated intracranial pressure (ICP) of unknown etiology. The investigators aim to study the quantitative D-dimer level and the role of anticoagulant therapy in the absence of occlusive sinus thrombosis in IIH patients.

NCT ID: NCT03963063 Completed - Anesthesia Clinical Trials

Neurological Effects of Goal-directed Fluid Therapy in Beach Chair Position Shoulder Surgery

Start date: June 27, 2019
Phase: N/A
Study type: Interventional

Patients receiving beach chair position shoulder surgery are vulnerable to perioperative cerebral desaturation, which is reported to be a risk factor for postoperative cognitive dysfunction. Investigators design this study to test the efficacy of perioperative goal-directed therapy in preventing cerebral desaturation and postoperative cognitive dysfunction in patients receiving beach chair position shoulder surgery.

NCT ID: NCT03962322 Completed - Clinical trials for Weaning From Mechanical Ventilation

Diaphragmatic Tissue Doppler During Weaning From Mechanical Ventilation

TDD-wean
Start date: May 27, 2019
Phase: N/A
Study type: Interventional

Weaning from mechanical ventilation is a critical issue and the diaphragmatic disfunction has been demonstrated to play an important role in extubation failure. the aim of present investigation is to evaluate diaphragmatic excursion velocity during in patients undergoing spontaneous breathing trial through tissue Doppler analysis in both inspiration and expiration.