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Clinical Trials/NL-OMON53254
NL-OMON53254
Not Yet Recruiting
N/A

Electromyography to assess the change in muscle activity as a result of intrathecal baclofen treatment - EMG in ITB

Overview

Phase
N/A
Intervention
Not specified
Conditions
Not specified
Sponsor
Erasmus MC, Universitair Medisch Centrum Rotterdam
Enrollment
32
Status
Not Yet Recruiting
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Observational non invasive

Investigators

Eligibility Criteria

Inclusion Criteria

  • Receiving an intrathecal baclofen trial (single shot baclofen test or
  • external intrathecal baclofen pump implantation) or permanent intrathecal
  • baclofen pump implantation
  • Unilateral or bilateral spasticity of lower limbs
  • Modified Ashworth Scale and electromyography measurements possible (18,5 \*
  • BMI \< 30\)
  • Able to understand and comply to verbal instructions

Exclusion Criteria

  • Age under 18 years old
  • High sensitivity of lower limb skin

Outcomes

Primary Outcomes

Not specified

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