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Reliability of Spasticity Measurement With Lokomat

O

Ospedale Generale Di Zona Moriggia-Pelascini

Status

Suspended

Conditions

Spasticity, Lokomat

Treatments

Other: L-stiff
Other: Ashworth

Study type

Observational

Funder types

Other

Identifiers

NCT02718053
spasticity01

Details and patient eligibility

About

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

Enrollment

20 estimated patients

Sex

All

Ages

18 to 80 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • patients affected by lower limbs spasticity

Exclusion criteria

  • medical contraindications to mobilization with Lokomat

Trial design

20 participants in 2 patient groups

spasticity
Description:
patients affected by spasticity of the lower limbs
Treatment:
Other: Ashworth
Other: L-stiff
controls
Description:
healthy subjects
Treatment:
Other: Ashworth
Other: L-stiff

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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