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NCT ID: NCT03112408 Completed - Cerebellum Disease Clinical Trials

Eye Movements and Visuo-spatial Perception

Start date: September 26, 2018
Phase: N/A
Study type: Interventional

This research aims to highlight the key roles of the cerebellar and cortical fronto-parietal networks in the coupling of eye movements with visual perception and visuo-spatial attention.

NCT ID: NCT03111849 Completed - COPD Clinical Trials

Sarcopenia in COPD Patients: a French Study

SARCOBS
Start date: January 2017
Phase:
Study type: Observational

The prevalence of sarcopenia is high in many organ pathologies such as COPD, but remains little studied in acute respiratory failure. Sarcopenia is a health problem representative of frailty, loss of autonomy and decreased muscle strength. The frequency and evolution of sarcopenia is unknown in patients having chronic bronchic obstruction with exacerbation.

NCT ID: NCT03111797 Completed - Cardiac Output Clinical Trials

Robot-assisted Lobectomy Versus Video-assisted Lobectomy

Start date: January 1, 2016
Phase:
Study type: Observational

This prospective and observational cohort studies the morphine consumption difference during the first 48 hours after a lung lobectomy between patients operated with a robot assisted or a video-assisted technique for a lung cancer lobectomy. Second outcome was to search eventual cardiac output difference during the surgery in 100 patients (50 in each group) using a non invasive monitoring device of cardiac output All patients operated between january 2016 and March 2017 for a lung cancer lobectomy were included.

NCT ID: NCT03111654 Completed - Atrial Fibrillation Clinical Trials

A Pilot Study on the Prevention of the Vascular RISK Related to Atrial Fibrillation After Intracranial Hemorrhage by Closing the Left Auricle

RIVAFAG
Start date: July 14, 2016
Phase: N/A
Study type: Interventional

Atrial fibrillation (AF) is a frequent heart rhythm disorder, responsible for the formation of cardiac thrombi, which can embolize in the systemic circulation, responsible for strokes (Cerebrovascular accidents). AF increases the risk of stroke and stroke-related disability. Preventing the thromboembolic risk associated with FMD is therefore a public health issue. The reference treatment is oral anticoagulation but this treatment is contraindicated in patients with a history of intracranial hemorrhage. The percutaneous closure of the auricle is a recent technique which makes it possible to exclude this appendix from the left atrium where the majority of thrombi are formed in the framework of the AF. Comparative studies have shown the effectiveness of this technique, appearing to be similar to that of anticoagulation. However, in view of the per-procedural risk, the indication of closure was retained by the health authorities only in the event of a contraindication to oral anticoagulants in patients with non-valvular AF with a high thromboembolic risk. Patients with a history of intracranial hemorrhage are therefore candidates for this technique, but there are few studies where these patients were included. The risk-benefit must be demonstrated over the long term, in terms of ischemic, hemorrhagic recurrence and becoming functional and cognitive.

NCT ID: NCT03111108 Completed - Clinical trials for Hepatitis C Virus (HCV) Infection

Efficacy and Safety of Elbasvir (MK-8742) + Grazoprevir (MK-5172) in Treatment-Naïve/Treatment-Experienced (TN/TE) French Participants With Hepatitis C Virus (HCV) Genotype 4 (GT4) Infection (MK-5172-096)

Start date: June 20, 2017
Phase: Phase 4
Study type: Interventional

The purpose of this study was to evaluate the efficacy of 8 and 12 weeks of treatment with a fixed dose combination (FDC) of elbasvir (EBR) 50 mg + grazoprevir (GZR) 100 mg (i.e., MK-5172A) as assessed by the percentage of participants with hepatitis C virus (HCV) genotype (GT) 4 infection that achieve sustained virologic response (HCV ribonucleic acid [RNA] < Lower Limit of Quantification [LLOQ]) 12 weeks after the end of study therapy (SVR12). This study also evaluated the safety and tolerability of EBR/GZR.

NCT ID: NCT03110458 Completed - Clinical trials for Acute Unilateral Vestibulopathy (AUV)

Efficacy of SENS-111 in Patients Suffering From Acute Unilateral Vestibulopathy

Start date: August 16, 2017
Phase: Phase 2
Study type: Interventional

A multicenter, randomized, double-blind, placebo-controlled study to assess the efficacy and safety of 2 dose-regimens of orally administered SENS-111 (100mg and 200mg) given during 4 days in patients suffering from Acute Unilateral Vestibulopathy (AUV)

NCT ID: NCT03110380 Completed - HIV-1-infection Clinical Trials

Switching to a Fixed Dose Combination of Bictegravir/Emtricitabine/Tenofovir Alafenamide (B/F/TAF) in Human Immunodeficiency Virus Type 1 (HIV-1) Infected Adults Who Are Virologically Suppressed

Start date: June 12, 2017
Phase: Phase 3
Study type: Interventional

The primary objective of this study is to evaluate the efficacy of switching from a regimen of either dolutegravir (DTG) and emtricitabine /tenofovir alafenamide (F/TAF) or DTG and emtricitabine/tenofovir disoproxil fumarate (F/TDF) to a fixed dose combination (FDC) of bictegravir/emtricitabine/tenofovir alafenamide (B/F/TAF) versus DTG+F/TAF in virologically suppressed HIV-1 infected adults with or without antiretroviral (ARV) resistance.

NCT ID: NCT03110094 Completed - Clinical trials for Rheumatoid Arthritis

Investigation of Immunological and Pharmacological Factors for Response to Adalimumab in Rheumatoid Arthritis

PROMETHEE
Start date: March 13, 2017
Phase: N/A
Study type: Interventional

Interventional study with minimal risks and constraints, prospective, mono-centric.

NCT ID: NCT03109275 Completed - Healthy Clinical Trials

Connectome Characterization With Aging

AGE-CONNECT
Start date: January 22, 2016
Phase: N/A
Study type: Interventional

The main aim of this project is to develop a new model to characterize brain connectivity and its changes with aging. This characterization will be based on new sensitive and specific markers, allowing a better understanding of structural and functional brain networks. To this end, two complementary MRI methods will be developed: 1) Resting-state functional MRI (rs-fMRI) which allows the measurement of cerebral activity in different cortical gray matter regions, and 2) high angular resolution diffusion imaging (HARDI) MRI, which allows to characterize brain tissue microarchitecture. HARDI sequences will be developed to acquire and reconstruct fiber tractography of patient's brains. In combination with conventional MRI, both HARDI and rs-fMRI will be used to estimate the connection degree between each pair of cortical regions, so- called "Connectome". Once generated, brain networks will be quantified through numerous graph metrics, such as graph density, global efficiency and assortativity (etc.), reflecting the organization and topology of subjects' connectivity with aging.

NCT ID: NCT03109080 Completed - Clinical trials for Radiotherapy Side Effect

Olaparib & Radiation Therapy for Patients Triple Negative Breast Cancer (TNBC)

RadioPARP
Start date: July 24, 2017
Phase: Phase 1
Study type: Interventional

A Phase I of Olaparib with Radiation Therapy in Patients With Inflammatory, Loco-regionally Advanced or Metastatic TNBC (triple negative breast cancer) or Patient With Operated TNBC with Residual Disease.