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Clinical Trials/DRKS00010413
DRKS00010413
Completed
未知

Comparison of the therapeutic benefit to combination therapy of botulinum neurotoxin and cast as well as single dose of botulinum neurotoxin on the wrist spasticity in different time intervals

eurologisches Rehabilitationszentrum Leipzig0 sites60 target enrollmentJune 7, 2016

Overview

Phase
未知
Intervention
Not specified
Conditions
G81.1
Sponsor
eurologisches Rehabilitationszentrum Leipzig
Enrollment
60
Status
Completed
Last Updated
last year

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
June 7, 2016
End Date
November 19, 2015
Last Updated
last year
Study Type
Interventional
Sex
All

Investigators

Sponsor
eurologisches Rehabilitationszentrum Leipzig

Eligibility Criteria

Inclusion Criteria

  • Aged 18 years \- stoke with spasticity of the upper limb \-MAS 2 \- 3 \- noticeable catch (according to Tardieu Scale) \-pROM wrist affected: \= 0 ° in extension

Exclusion Criteria

  • \- Age \<18 years \- MAS \= 1\+ or\> 3 \- wrist is not up to the 0 position (PROM) mobilized \- no meaningful catch (Tardieu Scale) \- fixed contracture of the fingers and / or wrist \- Serious additional diseases \- severe communication disorder \- myasthenia gravis, Lambert\-Eaton syndrome, ALS or other serious neuromuscular diseases \- severe dysphagia \- current administration of aminoglycosides \- proven hypersensitivity to Clostridium botulinum toxin A or any of the excipients of the preparation Dysport® \- Planned operations within the next 12 weeks ago \- pregnancy, lactation period \- anticoagulant therapy (Warfarin, Falithrom) \- infections in the injection area and skin damage in the area of ??castings \- Significant edematous swelling of the arm and hand \- Peri\-articular heterotrophic ossification in the investigation area \- Unstable fractures in the study area \- gout and diseases of rheumatic at the involved joints (upper limb)

Outcomes

Primary Outcomes

Not specified

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