Clinical Trials Logo

Muscle Spasticity clinical trials

View clinical trials related to Muscle Spasticity.

Filter by:

NCT ID: NCT02757404 Completed - Muscle Spasticity Clinical Trials

Meditoxin® Treatment in Patients With Post Stroke Upper Limb Spasticity

Start date: May 30, 2016
Phase: Phase 4
Study type: Interventional

Botulinum Toxin for the Treatment of Post Stroke Upper Limb Spasticity.

NCT ID: NCT02749591 Completed - Stroke Clinical Trials

Comparative Hybrid Effects of Combining BoNT-A With Robot-assisted or Mirror Therapy for U/E Spasticity Stroke Patients

Start date: May 2, 2016
Phase: Phase 3
Study type: Interventional

The aim of this study will be to determine and compare the immediate and longer-term effects of combination of BoNT-A injection and mirror therapy vs combination of BoNT-A injection and robot-assisted therapy.

NCT ID: NCT02736747 Active, not recruiting - Stroke Clinical Trials

Effects of Cryotherapy on Ankle Movements and Gait of Spastic Hemiparetic Subjects

Start date: April 2016
Phase: N/A
Study type: Interventional

The stroke has been described as the third cause of death and main cause of disability in the worldwide population. About 60% of the survivors are able to walk following the rehabilitation process, however deficits on lower limbs functions often persists in most cases, affecting the gait and functional mobility. In this sense, several interventions are applied in the clinical practice to optimize the functional performance. Cryotherapy is one of the most used techniques aiming to reduce spasticity temporarily, allowing the training of functional tasks, such as walking. The aim of the present study is to evaluate the immediate effects of cryotherapy (ice pack) on neuromuscular performance, proprioception, passive resistance of dorsiflexors and plantarflexors muscles, and also on gait performance in chronic post-stroke subjects. Eighteen chronic hemiparetic subjects will participate in this crossover placebo-controlled trial. The order of intervention (cryotherapy or placebo) will be randomized. Fifteen days of washout period will be considered. The cryotherapy/placebo will be applied on the posterior area of the leg for 20 minutes. Initially Fugl Meyer will be applied. All other assessments will be performed before and after intervention: spasticity level, classified according to Modified Ashworth Scale; temporo-spatial and angular parameters for trunk, hip, knee and ankle during gait, using a motion analysis system (Qualysis AB, Gothenburg, Sweden); the proprioception (joint position sense), passive resistance to stretching, isometric and isokinetic torques during contractions of plantarflexors and dorsiflexors of the ankle, evaluated through isokinetic dynamometer. Concomitantly, bilateral activation of soleus, gastrocnemius, tibialis anterior and peroneus will be assessed by electromyography during isokinetic dynamometer assessment and gait. The following electromyographic variables will be analyzed: maximum activation amplitude, muscle onset, coactivation index between agonists and antagonists. For statistical analysis, normality (Shapiro Wilk) and homogeneity (Levene) tests will be applied. If the variables have a distribution considered normal and homogeneous, Two-way ANOVA with repeated measures will be applied. Otherwise, non-parametric statistics (Friedman test) will be applied. A significance level of 0.05 will be considered for all statistical tests.

NCT ID: NCT02719483 Completed - Cerebral Palsy Clinical Trials

Radial Extracorporeal Shock Wave Therapy for Spastic Plantar Flexor Muscles in Young Children With Cerebral Palsy

Start date: April 2014
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether radial extracorporeal shock wave therapy in combination with traditional physical therapy is safe and effective for the management of spastic plantar flexor muscles in patients with cerebral palsy younger than averaged three years of age.

NCT ID: NCT02718690 Completed - Spasticity Clinical Trials

Importance of the Current Density in TENS

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

The purpose of this study is demonstrate the importance of density current of TENS in the effect about H-reflex in healthy volunteers.

NCT ID: NCT02718053 Suspended - Spasticity, Lokomat Clinical Trials

Reliability of Spasticity Measurement With Lokomat

Start date: July 2015
Phase: N/A
Study type: Observational

The purpose of the study is to evaluate the reliability of spasticity measurement with Lokomat

NCT ID: NCT02663206 Withdrawn - Clinical trials for Esophageal Achalasia

Peroral Endoscopic Myotomy Versus Botulinum Toxin Injection in Spastic Esophageal Disorders

Start date: September 2016
Phase: N/A
Study type: Interventional

To compare the efficacy of peroral endoscopic myotomy and Botulinum toxin injection in spastic esophageal disorders.

NCT ID: NCT02655471 Completed - Clinical trials for Tropical Spastic Paraparesis

Effect of Raltegravir in Patients With Acute Tropical Spastic Paraparesis - Human T-Lymphotropic Virus 1 Infection

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

This is a pilot study of intervention in a group of patients with tropical spastic paraparesis/ myelopathy to evaluate virologic and clinical response of raltegravir plus zidovudine in this group of patients.

NCT ID: NCT02643160 Completed - Clinical trials for Cerebral Palsy, Spastic

Analyzing the Effect of Trunk Training on Limbs in Children With Spastic Cerebral Palsy

FTT
Start date: January 2014
Phase: N/A
Study type: Interventional

The purpose of this study is to analyze if trunk training has effects on trunk, upper, lower extremity motor functions in children with spastic Cerebral Palsy. Second purpose is to analyze the relation between trunk control and prematurity, birth weight, upper and lower extremity motor functions in children with spastic Cerebral Palsy.

NCT ID: NCT02610387 Recruiting - Ischemic Stroke Clinical Trials

The Effects of tDCS Combined With Balance Training on Lower Limbs Spasticity in Chronic Stroke Patients

Start date: September 12, 2016
Phase: N/A
Study type: Interventional

Spasticity is one of the most common disorders in patients with central nervous system diseases such as stroke. Transcranial direct current stimulation stimulation (tDCS) is a noninvasive tool that can be used to modulate cortical excitability of the leg motor area, and the spinal motor circuits as well. Objective:The objectives of this study is to examine the efficacy of anodal tDCS combined with Biodex balance training on lower limbs spasticity in chronic stroke patients using laboratory and clinical assessments.