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Muscle Spasticity clinical trials

View clinical trials related to Muscle Spasticity.

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NCT ID: NCT02166541 Completed - Clinical trials for Spastic Diplegia Cerebral Palsy

Evaluation of INRS With BCSK in Children With Spastic Bilateral Cerebral Palsy: a Randomized Controlled Trial.

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

A randomized control trial investigating "Biomechanical Correction of the Spine according to Kozyavkin" (BCSK) which is a part of the treatment concept "Intensive Neurophysiological Rehabilitation System" (INRS). BCSK is used with the aims to reduce muscle tone and improve gross and fine motor function in children with Spastic Bilateral Cerebral Palsy.

NCT ID: NCT02145689 Withdrawn - Stroke Clinical Trials

Long-Term Study of OnabotulinumtoxinA Treatment in Adult Patients With Upper Limb Spasticity

Start date: August 2014
Phase: Phase 3
Study type: Interventional

This is a long-term safety and efficacy study of onabotulinumtoxinA in poststroke patients with upper limb spasticity.

NCT ID: NCT02145676 Terminated - Stroke Clinical Trials

OnabotulinumtoxinA Treatment in Adult Patients With Upper Limb Spasticity

Start date: May 2014
Phase: Phase 3
Study type: Interventional

This is a safety and efficacy study of onabotulinumtoxinA in poststroke patients with upper limb spasticity.

NCT ID: NCT02145650 Withdrawn - Muscle Spasticity Clinical Trials

Spasticity Registry Evaluating Epidemiology, Treatment Patterns and Clinical Needs

STRETCh
Start date: May 2014
Phase: N/A
Study type: Observational

This study will examine the epidemiology (incidence and control of a disease), burden, clinical need, and treatment patterns of spasticity in patients with a diagnosis of Cerebral Palsy (CP), Multiple Sclerosis (MS), Stroke, Spinal Cord Injury (SCI), or Traumatic Brain Injury (TBI).

NCT ID: NCT02127606 Recruiting - Spinal Cord Injury Clinical Trials

The Effect of Whole Body Vibration on Spasticity in Persons With Spinal Cord Injury

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

Extended periods of tilt table standing have been observed to improve spasticity in individuals with spinal cord injury (SCI). The purpose of this study is to determine the effect of three sessions of whole body vibration while tilt table standing on spasticity in individuals with a complete or incomplete SCI above the neurological level of T10. Participants in this study will undergo whole body vibration while standing on a tilt table for a total of approximately 14 minutes for a total of 3 sessions on 3 separate days. Spasticity monitoring will be evaluated prior to and after the intervention with the Modified Penn Spasm Frequency Scale, an interview to obtain the individual's perception and impression of the effect of whole body vibration on the performance of activities of daily living, quality of life, pain scale, and global impression of change.

NCT ID: NCT02114736 Recruiting - Stroke Clinical Trials

Rectus Femoris Tenotomy Versus Botulinum Toxin A for Stiff Knee Gait After Stroke

Start date: March 2014
Phase: Phase 4
Study type: Interventional

Stiff knee gait is defined as the lack of knee flexion in the swing phase of gait. Stiff knee gait is a frequent condition among stroke patients leading to reduce gait speed and increase energy cost. In association with neuro-rehabilitation, botulinum toxin A injections in the rectus femoris is recommended. However, the botulinum toxin A effect is transient necessitating repeated injections. The aim of this study is to compare the benefit of the rectus femoris tenotomy in comparison with botulinum toxin A injections according to the 3 domains of the International Classification of Functioning Disability and Health of the World Health Organisation

NCT ID: NCT02106351 Completed - Clinical trials for Upper Limb Spasticity (Altered Skeletal Muscle Performance) in Children

Efficacy And Safety Of Dysport In The Treatment Of Upper Limb Spasticity In Children

PUL
Start date: April 2014
Phase: Phase 3
Study type: Interventional

The purpose of this study is to assess the efficacy and safety of multiple doses of Dysport used in the treatment of upper limb spasticity (altered skeletal muscle performance) in children with cerebral palsy (CP).

NCT ID: NCT02085642 Recruiting - Stroke Clinical Trials

Investigation of the Use of Acupuncture for the Treatment of Spasticity in Chronic Stroke Participants

HHSCSTROKEAC
Start date: March 2015
Phase: N/A
Study type: Interventional

The purpose of this study is to investigate if acupuncture is more effective than sham treatment in reducing lower extremity spasticity, and improving gait speed in the chronic phase of stroke recovery.

NCT ID: NCT02074150 Not yet recruiting - Clinical trials for Upper Limb Spasticity Unilaterally in Adults With History of Stroke

ASIS for Botox in Upper Limb Spasticity

ASISinULS
Start date: January 2016
Phase: Phase 1/Phase 2
Study type: Interventional

Botox act on nerve endings, yet there are no nerve endings inside the muscle, where they are typically injected. All nerves terminate on the fascia, where ASIS device can precisely deliver Botox by creating that subdermal bloodless space, between the skin and muscle. Thus enhancing and prolonging Botox's efficacy, at the same time prevent it's unnecessary adverse reactions and distant spread, especially since Botox has no reason to travel to the rest of the body any way.

NCT ID: NCT02073513 Completed - Spasticity Clinical Trials

Kinesiotaping the Hand in Cerebral Palsy

Start date: November 2009
Phase: N/A
Study type: Interventional

BACKROUNDS: Thumb in palm deformity restricts hand function by prevent somatosensory input in the children with cerebral palsy who have spasticity in their hands. OBJECTİVES: To investigate the effects of thenar palmar kinesiotape application with and without pressure on hand function in children with cerebral palsy. METHOD: 45 children were randomly allocated to one of the thenar taping groups either with or without pressure or to the control group. Nine hole peg test and nine parts puzzle test were used to measure hand function. The two study groups were evaluated initially, with taping 20 minutes later and 20 minutes after taping was removed.