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Stroke clinical trials

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NCT ID: NCT04057690 Recruiting - Stroke, Acute Clinical Trials

Automatic PredICtion of Edema After Stroke

APICES
Start date: April 1, 2019
Phase:
Study type: Observational

To use machine learning for early detection of malignant brain edema in patients with MCA ischemia

NCT ID: NCT04055766 Not yet recruiting - Stroke Clinical Trials

A Diagnostic Test on DeepDoc-an AI-based Decision Support System

Start date: September 1, 2020
Phase:
Study type: Observational [Patient Registry]

DeepDoc is an AI-based decision support system for the early etiology diagnosis of neurological diseases using clinical data points from patients admitted to hospital within 24 hours.This study aims to evaluate whether the diagnosis of the DeepDoc AI-based decision support system is better than the doctor's initial diagnosis by a multi-center, superiority diagnostic study.

NCT ID: NCT04055597 Recruiting - Stroke Clinical Trials

Effects of Upper Extremity Rehabilitation Robot and Transcranial Direct Current Stimulation Among Patients With Stroke

Start date: June 1, 2017
Phase: N/A
Study type: Interventional

Effects of upper extremity rehabilitation robot and transcranial direct current stimulation on upper extremity function among subjects with tremor after stroke

NCT ID: NCT04054739 Completed - Stroke Clinical Trials

Cortical Activity and Gait Function for Robotic Gait Training in Hemiparetic Stroke

Start date: September 1, 2018
Phase: N/A
Study type: Interventional

Effects of robot-assisted gait training on cortical activity and gait function in hemiparetic stroke

NCT ID: NCT04054700 Recruiting - Stroke Clinical Trials

The Effect of Application of Proximal and Distal Upper Rehabilitation Robot With Stroke Patients

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

Comparison of the effect of upper limb rehabilitation on the application of proximal upper rehabilitation robot and distal upper rehabilitation robot with stroke patients

NCT ID: NCT04054102 Recruiting - Stroke Clinical Trials

Effects of Upper Extremity Rehabilitation Robot and Transcranial Direct Current Stimulation in Subacute Stroke

Start date: May 1, 2018
Phase: N/A
Study type: Interventional

Comparison of real transcranial direct current stimulation (tDCS) and sham tDCS combined with robot training for upper extremity rehabilitation.

NCT ID: NCT04052178 Completed - Stroke Clinical Trials

Sensory Neuromodulation Protocol for the Treatment of Post-stroke Oropharyngeal Dysphagia.

FIS2014
Start date: February 10, 2016
Phase: N/A
Study type: Interventional

Study design: Multicenter, experimental, randomized, crossed, double blind study (patient and results analysis). Aim: To evaluate the effect of different neurostimulation techniques on the neurophysiological and biomechanical swallowing mechanisms of patients with dysphagia associated with chronic stroke and select those techniques with the best results to be evaluated in the second phase of the study (medium-term effects). Outcome measures: - Videofluoroscopy: prevalence of impaired efficacy and safety of swallow (penetrations and aspirations), penetration aspiration scale (PAS: from 0 to 8), biomechanical parameters (time to laryngeal vestibule closure, upper esophageal sphincter opening). - Pharyngeal sensory evoked potentials (pSEP): latency and amplitude of obtained evoked potentials. Higher latency (0 onwards) means worse outcome and higher amplitude (0 onwards) means better outcome. - Pharyngeal motor evoked potentials (pMEP): latency, amplitude, duration and area of obtained evoked potentials. Higher latency (0 onwards) means worse outcome and higher amplitude (0 onwards) means better outcome. Treatments and patients: 36 post-stroke patients with oropharyngeal dysphagia (PAS superior or equal to 2) randomized patients in 3 treatment arms (3 groups of 12 patients). - Active and sham repetitive transcranial magnetic stimulation (rTMS): 90% of the resting motor threshold, 1250 pulses, 5 Hz. - Active and sham Intrapharyngeal Electrical Stimulation (PES): 75% of tolerance threshold, pulses of 0.2 ms, 5 Hz, 10 min. - Oral Capsaicin (active intervention, 10-5M, TRPV1 agonist) and placebo solution (sham): 100 mL, single administration. Administration of study therapies: The study will be performed in two visits separated for one week. In each visit patients will randomly receive active or sham treatment and a pre-post evaluation of biomechanics of deglutition (with VFS) and neurophysiological mechanisms (swallowing afferent and efferent pathways) will be performed in each visit. Acute randomized administration -> 1 active session (pre/post evaluation with VFS/pSEP/pMEP) + 1 separate control session 1 week apart (pre/post evaluation with VFS/pSEP/pMEP).

NCT ID: NCT04051671 Completed - Stroke Clinical Trials

Effects of Dual-transcranial Direct Current Stimulation During Physical Therapy in Sub-acute Stroke

Start date: August 6, 2019
Phase: N/A
Study type: Interventional

The aim of the present study is to evaluate the possible effect of using dual-tDCS applied during conventional physical therapy on lower limb function in stroke patients.

NCT ID: NCT04051658 Completed - Stroke Clinical Trials

Hemodynamic Response and Motor Functions Following Transcranial Direct Current Stimulation in Acute Stroke

Start date: August 6, 2019
Phase: N/A
Study type: Interventional

The aim of the present study is to evaluate the possible effect of using dual-tDCS applied before conventional physical therapy on motor functions and hemodynamic response

NCT ID: NCT04050917 Completed - Stroke Clinical Trials

Smartwatch App for Vibration Stimulation

Start date: July 17, 2019
Phase: N/A
Study type: Interventional

The objective of this study is to determine if the acute effect of vibration from a smartwatch on hand function is comparable to the effect of an existing laboratory prototype.