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Stroke clinical trials

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NCT ID: NCT02972008 Recruiting - Stroke Clinical Trials

Identification of Epigenetic Risk Factors for Ischemic Complication During the TAVR Procedure in the Elderly

METHYSTROKE
Start date: March 9, 2017
Phase:
Study type: Observational

Over the past ten years, the number of endovascular procedures has increased by 5% per year in Europe with the development of interventional cardiology, such as percutaneous coronary angioplasty, aortic valve replacements (TAVR), and vascular endoprosthesis. The neurological lesions detected on cerebral MRI caused by these endovascular procedures are frequent with an incidence of about 30-70%. These events, although subclinical, have an impact on morbidity and mortality and especially on long-term cognitive decline. TAVR is the reference treatment for symptomatic elderly patients with stenosis of the aortic valve, considered by a multidisciplinary "Heart Team" as at high surgical risk due to comorbidities, age and high perioperative risk scores ( Euroscore 2 and STS scores). Despite the net clinical benefit, an increase of silent neurological events was detected on post-procedural cerebral MRI with an incidence of approximately 70%. The epigenetic involvement in the occurrence of ischemic cerebral lesions is still largely unknown. Epigenetic mechanisms, such as DNA methylation, can be associated with aging processes and modulate the risk of developing cerebrovascular pathologies. They are likely to provide new biomarkers that predict the risk of brain damage. Hypomethylation of leukocyte DNA is directly related to atherosclerosis in humans. This hypomethylation of DNA would represent an easily measurable marker reflecting the presence and progression of atherosclerosis. Because atherosclerotic lesions often precede the clinical manifestation of ischemic cardiovascular disease, such as ischemic heart disease and stroke, DNA hypomethylation could be used to identify individuals at risk for cerebrovascular events. The investigator hypothesize that hypomethylation of leukocyte DNA can predict the risk of developing new ischemic brain lesions especially after a TAVI procedure.

NCT ID: NCT02971826 Recruiting - Stroke Clinical Trials

Use of the Thrombectomy Device ReViveā„¢ SE in the Acute Treatment of Stroke

REVIVE SE
Start date: November 30, 2018
Phase: N/A
Study type: Interventional

The last marketed thrombectomy devices, named stentretriever, permit a better and faster recanalization in patient with a stroke. The REVIVETM SE is a device designed to restore the brain perfusion in patient with an intracranial artery occlusion. The REVIVETM Se device is not widely use in Europe and in France. The objective of this study is to assess the interest of using this device in the standard care of ischemic stroke in the radiology unit of the hospital Pierre Wertheimer, Lyon. The medical care will not be modified but data will be collected in order to determine whether or not this device is useful for the practice of the radiology unit.

NCT ID: NCT02971774 Recruiting - Clinical trials for Stroke in Patients: New Tool to Evaluate the Impact in Their Life

Development of a Multimodal Approach to Assess Stroke Patients Daily Life Activities

Start date: January 2017
Phase:
Study type: Observational

The aim of the study consists in enriching knowledge of health professionals, on the functional difficulties encountered by hemiplegic patients outside the hospital, in particular on hobbies, going out with friends or family, work, daily life and the personal projects. Another objective is to evaluate the diversity of the attitudes and representations of the patients about their body damage. Lastly, the study seeks to develop a new grid of evaluation of the quality of life of the patients, which determines more fields of the existence significantly impacted by the hemiparesy, from the point of view of the patients. It is a question of improving the therapeutic care of the patients and to determine if various therapeutic approaches (occupational, pharmacological, surgical) have an impact on these various fields. The study will be based on qualitative data (interviews) and quantitative (questionnaires).

NCT ID: NCT02960737 Recruiting - Stroke Clinical Trials

Dysphagia Evaluation After Stroke- Effect Oral Neuromuscular Training on Swallowing Dysfunction

DESIRE
Start date: December 1, 2022
Phase: N/A
Study type: Interventional

The aim of this study is to investigate the effect of a specific rehabilitation program with an oral device used in stroke patients with persistent oral-and pharyngeal dysphagia.

NCT ID: NCT02960009 Recruiting - Stroke Clinical Trials

Motor Excitability Study of High Definition Transcranial Direct Current Stimulation (HD-tDCS) in Chronic Stroke

Start date: June 20, 2016
Phase: N/A
Study type: Interventional

High definition tDCS will be conducted to both stroke and healthy subjects on primary motor cortex area to explore the motor excitability changes before and after stimulation. In next stage, a randomized control trial with 20-session training will be conducted to evaluate the effectiveness of transient modulation of cortical excitability through multisite HD-tDCS with EMG driven robot hand training, a sham stimulation with EMG-driven robot hand training will be applied as control group.

NCT ID: NCT02938416 Recruiting - Stroke Clinical Trials

The Effect of Isokinetic Strengthening Training

Start date: January 2013
Phase: N/A
Study type: Interventional

Our participants will include 40 patients within one month of stroke, 43 patients who received total hip replacement or total knee replacement two to four weeks before. The participants will be randomly assigned to isokinetic, isotonic or isometric training groups. Outcome measures including isometric peak torque of hip/knee at 90 degree of flexion, peak torque of hip/knee at angular velocity of 60 degree/s and 120 degree/s, Short Form 36 (SF-36), the Timed Up and Go test, the Oxford Hip/knee Score, the plasma concentration of hsCRP, and the level of substance P in saliva will be collected at the beginning and 4 weeks after the training program. Statistical significant differences will be determined between the improvement of outcome measures of the isokinetic and the isotonic training groups.

NCT ID: NCT02923752 Recruiting - Ischemic Stroke Clinical Trials

Whole Brain Vessel Wall Imaging in Stroke Patients (WISP): An International Multi-Center Registry

WISP
Start date: February 1, 2017
Phase:
Study type: Observational

This is a new vessel wall imaging-based stroke registry which will investigate the clinical utility of the whole-brain intracranial vessel wall Magnetic Resonance Imaging (MRI) technique in assessing the etiologies in patients with ischemic stroke.

NCT ID: NCT02902393 Recruiting - Stroke Clinical Trials

Interest of Thromboelastography (ROTEM) as a Biomarker of Revascularisation in Stroke

ROTEMPredict
Start date: July 2016
Phase: N/A
Study type: Observational

Revascularisation using recombinant tPA is the reference treatment of stroke. However, the efficacy of fibrinolysis is about 50%. Several factors, including the size of thrombus, have been associated with revascularisation efficacy. The aim of this prospective study is to evaluate ex vivo the effect of tPA in patients with stroke with thromboelastography and to correlate results with the clinical outcome of patients. Results may predict revascularisation in patients with stroke.

NCT ID: NCT02902367 Recruiting - Acute Stroke Clinical Trials

Sms-guided Training After Acute Stroke or Transient Ischemic Attack - a Randomized Controlled Trial

SMS/TIA
Start date: November 2016
Phase: N/A
Study type: Interventional

Eighty community-living individuals in Uppsala municipality will be included. Intervention: Outdoor walking exercise program and one strength exercise. Methods: Clinical assessments, questionnaires and medical records. Assessment of motor function, cognition, level of physical activity, food intake and perceived stress are performed at screening as baseline measurements. Walking capacity, mobility, handgrip strength, body composition and cardiovascular risk markers will be assessed at baseline and after 12 week of training. At one year after training health-related quality of life, another cardiovascular incidence and mortality will be documented.

NCT ID: NCT02900521 Recruiting - Stroke Clinical Trials

Population-based Brest Stroke Registry

BREST
Start date: January 2008
Phase:
Study type: Observational [Patient Registry]

The registry is the main objective exhaustive list of cases validated stroke brain on a geographical area defined to calculate an incidence.