Hemiplegia Clinical Trial
Official title:
Effect of Botulinum Toxin Injections on Motor and Functional Ability of Upper Limb in Adults at Earlier Phases of Spastic Hemiplegia After Stroke
Botulinum toxin produced beneficial effects in spasticity in the hemiplegic upper limb. This study will test if botulinum toxin injections at earlier phases (<or = 3 months) in spasticity improve functional and motor tests compared with late injections (>or = 6 months).
Status | Recruiting |
Enrollment | 180 |
Est. completion date | December 2009 |
Est. primary completion date | January 2009 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Minimum age 18 - Spastic hemiplegia after ischemic stroke (carotid occlusion) within the past 3 months. - Antispasticity medication stabilized for the last 30 days - Severe cognitive impairment such that patient is unable to provide scale assessment. - Significant spasticity impeding improvement by re-education for 2 months or less - Lack of muscular retraction defined by a minimal range of articular motion as : - finger : complete extension and rolling up - wrist : extension 40°/flexion : 45° - elbow : extension - 10°/flexion : 120° - shoulder : Enjalbert score 2 or more - Antagonist muscles (to spasticity) activity score 1 or more - Social Security benefits Exclusion Criteria: - Ischemic stroke thought to be due to basilar or vertebral vessel occlusion - Known motor neuron or neuromuscular junction disease, disorders in which pain limits the ability to inject muscles (algodystrophy) - Absence of mobility in proximal part of upper limb that does not predict a functional gain - Minor stroke with non-disabling deficit or rapidly improving motor symptoms - other serious illness, e.g. severe hepatic, cardiac, or renal failure ; acute myocardial infarction ; or a complex disease that may confound treatment assessment - Treatment of spasticity by previous administration of botulinum toxin, if known - Known allergy to botulinum toxin - Currently participating in other research studies |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
France | Clermont-Ferrand University Hospital | Clermont-Ferrand | Auvergne |
Lead Sponsor | Collaborator |
---|---|
University Hospital, Clermont-Ferrand | Center of Physical Medicine and Rehabilitation (Notre Dame de Lourdes Center in Rennes), Centre Hospitalier Universitaire de Besancon, Centre Hospitalier Universitaire de Saint Etienne, Centre Régional de Département de médecine physique et réadaptation CHU-C3RF in Angers, J. Rebeyrol Hospital in Limoges, Rennes University Hospital, Saint Jacques Hospital in Nantes |
France,
Wissel J, Müller J, Dressnandt J, Heinen F, Naumann M, Topka H, Poewe W. Management of spasticity associated pain with botulinum toxin A. J Pain Symptom Manage. 2000 Jul;20(1):44-9. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Deficiency, incapacity, handicap : Frenchay Arm test(post stroke arm function); Enjalbert test; | |||
Primary | Box and blocks test | |||
Primary | Enjalbert test | |||
Primary | Modified Ashworth scale (upper limb) | |||
Primary | Functional Independence Measure | |||
Primary | Fugl-Meyer upper limb test | |||
Primary | Clinical Global Impression (CGI) | |||
Primary | 36-Item Short Form (SF-36) quality of life | |||
Secondary | Range of pain | |||
Secondary | Individual functional kinesitherapy |
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